Sciencemadness Discussion Board

cinnamon oil to benzaldehyde

questions - 15-6-2011 at 01:09

My lab was at my friends house and we did our little experiments in his garage. Unfortunately his mother has found a new guy and he is now living in the house and has started asking questions about us. I cant experiment in there anymore and it would be far too difficult for me to do it anywhere else. Also, I'm still living at home with my parents and they'd kill me if they sore me doing those sort of things :(
Thus I'm hoping to find people who have already done these things and can help me out, it sucks I know :(

EDIT by Nicodem: I split questions' off topic posts from the toluene --> benzaldehyde thread and the replies, and merged them in this thread he finally created for his questions.

[Edited on 25/12/2011 by Nicodem]

benzaldehyde from cinnamon oil

questions - 26-8-2011 at 15:59

Quote: Originally posted by CycloKnight  
Hi peeps, been off the forum a good while but its good to be back :).

I’ve significantly improved the original batch method I posted last year, what follows is my latest method.

This approach uses the same setup as the last steam distillation variation graphically depicted in in this thread.

Basically, the items used were:
hot plate, pressure cooker steam generator & associated tubing, etc
3L 3-neck RBF & mantle
vigreux column, right angle bend & still head
condenser
Vacuum pump & glassware for purfying the final product & recycling unreacted cinnamaldehyde.

chemicals: 2 litres tap water, lecithin, cinnamon oil, NaOH

Essentially, a large reaction vessel and a means of steam & vacuum distilling are all the equipment really required.


Begin by setting up all equipment, add 2 L water & ~1.5g lecithin.
The first variation is to use OTC sodium hydroxide instead of sodium carbonate, simply add the alkali to adjust the pH within the range of 12-13, only small amounts are required.

The second variation is to slowly drip in the cinnamon oil during the course of the reaction, the benzaldehyde being steam distilled as it forms. Begin the addition once the pH adjusted solution has heated to boling temperature and the steam is passing though the solution.

The third variation is to stop the cinnamon oil addition after 5 min, then check the distillate. If benzaldehyde is clearly distilling over, then continue with the addition.
A crude test is to simply taste the steam distillate as it drips into the receiving vessel, if it burns your tongue off, then you're doing well. If it tastes sweet, then significant quantities of cinnamon are being carried over. Should this not change after a short while, then double check the pH !

Provided that the pH is correct and the cinnamaldehyde content is high (70%+) then benzaldehyde laden distillate should start collecting almost immediately after the addition has begun.
However, if it is not, wait for the benzadehyde to start collecting, THEN continue with the addition. This prevents unnecessary amounts of cinnamaldehyde being steam distilled at the start of the process, which is a serious problem with the old batch mode reaction.

Note that by slowly dripping the cinnamon oil instead of adding it all at once to the reaction mix, single run conversion is increased by 20-30%.

Ensure the rate of cinnamon oil drip rate is approximately equivalent to the quantity of oil being steam distilled, thus maintaining high dilution in the reaction mixture.

After 300 to 500 ml of cinnamon oil had been added, the drip rate is stopped and the steam distillation continued until all the aldehyde has been steam distilled from the reaction mix. If using less than 2L of water, then adjust proportionally to maintain the same dilution. At this point, dump the mix and replace with clean pH adusted water with at least ~1.5g lecithin.
This step removes tar and other junk that slows down the reaction and reduces benzaldehyde production. Significantly reduced tar formation will also result from periodically carrying out this step (very imporant if high yields are desired).
Also note that with this method, the pH tends to slowly drop over time during the course of the steam distillation, so check the pH every couple hours, and top up with NaOH if and when required. Its preferable to simply add small amounts concentrated NaOH solution when topping up, using a dropper makes the alkali addition much simpler since NaOH pellets will rapidly collect moisture and stick to the sides of the reaction vessel.

Efficiency is further improved if the steam distillate (after oil separation) is also extracted with DCM, though this isn't absolutely necessary.

Once the the product oil is pooled, vacuum distillation will remove the benzaldehyde - no need to vacuum distill the recycle cinnamon aldehyde, just drip it into the steam distillation vessel, just as with the cinnamon oil feed. Expect the quantity of unreacted cinnamon aldehyde to be circa 25%, but if the reaction mix was kept clean during the process then it may be considerably less. The benzaldehyde distillate is clear, & much purer than the original solvent extraction method that doesn't employ the steam distillation. Give the batch solvent extraction a rest folks, use the steam distillation variation if producing benzaldehyde from cinnamon oil!
Far, far less work.

Using the above approach, overall molar conversion to benzdehyde is at least 80%.

I’ve managed higher conversion efficiencies (~90%), but the reaction efficiency is subject to variation according to varying reaction conditions, i.e. feed rate, reaction mix volume (i.e. dilution), and the quantity of cinnamon oil fed to the reaction mix before changing the solution. >80% seems to be a realistic overall figure.

Also...
Remember to keep the reaction mix free of tar & cinnamon oil impurities as much as possible to give consistent high yields.

If dripping the aldehyde into the mixture isn't practical for any reason, you can periodically add the cinnamon oil in small batches, say 20-50 ml at a time to give good conversion, but expect a little more cinnamonaldehyde to distill over.


OK, here cyclonknight described an attractive process for making benzaldehyde from cinnamon oil by slowly dripping the cinnamon oil into the already boiling water with dissolved NaOH at around a PH of 12 to 13.
What I dont understand is that on the wikipedia they say that benzaldehyde is converted into two other chemicals when exposed to highly concentrated NaOH, and I quote

"Benzaldehyde undergoes disproportionation upon treatment with concentrated alkali (Cannizzaro reaction): one molecule of the aldehyde is reduced to the corresponding alcohol and another molecule is simultaneously oxidized to sodium benzoate."

So if the cinnamon oil is being converted to benzaldehyde, and is steam disstilled out, why isn't the benzaldehyde being converted into other products as described by the wikkipedia?

redox - 27-8-2011 at 06:59

A concentrated solution of NaOH will in fact disproportionate aldehydes. However, this is by far not a concentrated solution. If you notice, Cycloknight said "only small amounts [of NaOH] are required." A concentrated solution of NaOH will be pH 14, whereas a very dilute solution will be 12-13.

Thus, the Cannizzaro shouldn't occur very readily in these conditions.

MeSynth - 27-8-2011 at 16:45

Quote: Originally posted by questions  
Quote: Originally posted by CycloKnight  
OK, here cyclonknight described an attractive process for making benzaldehyde from cinnamon oil by...



This is the easiest way (best)!! A while back I dismissed this method due to there being no cinnamaldehyde available. I just found a source of trans-cinnamaldehyde. Does anyone know if it will work for the trans isomer of cinnamaldehyde? Does anyone know of a good source of cinnamaldehyde? :cool:

[Edited on 28-8-2011 by MeSynth]

MeSynth - 27-8-2011 at 16:59

trans-Cinnamaldehyde is the molecule that occurs in nature so it will work with trans-Cinnamaldehyde since this is what is found in essential oil of cinnamon.

MeSynth - 27-8-2011 at 17:38

Here is the actual example described in the patent used by cyclo.

-------------------------------------------------------------------------------------------------

EXAMPLE II

Preparation of Natural Cinnamaldehyde and Natural Benzaldehyde

Into a three neck flask equipped with stirrer, thermometer and reflux condenser is placed 10 grams of cassia oil and 100 ml of a 3% aqueous sodium carbonate solution. Boiling chips are added and a water-washed stream of nitrogen is passed over the reaction mass to help prevent oxidation of the formed benzaldehyde. The mixture is heated to reflux and refluxed for a period of 7 hours (100° C.). The resulting material contains 70% benzaldehyde and 30% cinnamaldehyde.

-------------------------------------------------------------------------------------------

Cassia oil is not pure cinnamaldehyde so it is more than likely that you would want to use less cinnamaldehyde if that is what your using for the reaction. In the pattent they said their cassia oil contained 88% cinnamaldehyde. That means that only 8.8 garms of cinnamaldehyde was used.
to prevent oxidation of the benzaldehyde they used a water washed stream of nitrogen. The lose of benzaldehyde to oxidation shouldn't be so bad that you need a stream of nitrogen.

questions - 27-8-2011 at 18:07

What I hate about making benzaldehyde from cinnamon oil is that is is very difficult to separate the benzfrom the cinamon and so usually a solvent based extraction must be employed about four times followed by a vacuum disstilation. If you ask me it's still alot of work and the process requires the right equipment and glassware.
If we could find a way to separate the benzaldehyde from the cinnamon oil without the need of vacuum disstillation than that would make the process much easyer and using sodium metabisulfite is not a good idea to recover the benzaldehyde because it will also form a duct with the cinnamon aldehyde, for it's name suggests it to is an aldehyde :(

MeSynth - 27-8-2011 at 20:03

The sodium bisulfide method could work. Benzaldehyde has a boiling point that is close to 50 degrees less than that of cinnamaldehyde. So when the crystals are heated to 170 degrees the benzaldehyde will boil out while the cinnamaldehyde will just liquify (in theory). I have not read about the effects of heating the sodium bisulfide adduct of cinnamaldehyde and I have not had the pleasure of conducting any tests so for all I know the crystals will explode.

MeSynth - 27-8-2011 at 20:14

Here is a relatively usless link. http://www.scientific.net/AMR.183-185.1942

You will find a little more info about the sodium bisulfide adduct of cinnamaldehyde.

-------------------------------------------------------------

And here is a post by: arsphenamine
in the forum titled: Cinnamaldehyde from cinnamon bark powder
_

Aldehydes have classically been purified by precipitation of the bisulfite adduct, filtration and washing of the solid, and regeneration by gentle hydrolysis with bicarbonate or acid as circumstances dictate.

TLC roughly shows you how impure it is. GC exactly shows you, but doing TLC using coffee filter strips is often all you need.

You can purify by vacuum distillation if you need something analytically pure although you lose some product to the pot.

OrgSynth has a good prep for 3-methyl phenylpropanal.

The money shot:

A completely pure sample of the aldehyde is readily obtained by stirring the crude aldehyde with excess saturated aqueous sodium bisulfite solution for several hours, filtering the solid bisulfite adduct, washing with ether, and liberating the aldehyde with excess aqueous sodium bicarbonate.


------------------------------------------------------------------

From what I read above I found that I can purify a crude mixture of aldehyde by a sodium bisulfide adduct. This is however not going to separate the benzaldehyde from the cinnamaldehyde and aldehyde. So far the only way I can imagine is fractional distillation which is probably the best way.

[Edited on 28-8-2011 by MeSynth]

Check this clip out! I got it from patent #4673766

___


In a preferred mode of conducting the method, the cinnamaldehyde is dispersed in the water in the presence of shearing agitation and a surfactant. In another aspect of this invention, it is preferred to employ an anionic surfactant such as sodium lauryl sulfate. Preferably, the hydroxide ion is furnished by means of sodium hydroxide which also achieves the pH in the range of about 11 to about 13. It has critically been determined that the fractional steam distillation of benzaldehyde from the cinnamaldehyde must be conducted at a pH within the range of about 11 to about 13, preferably about 12 to about 12.5. Below and above this pH range, very poor conversions are obtained of 50% or far less and competing reactions interfere with the production of benzaldehyde. Outside of this critical pH range, side reactions, polymerization and other adverse reactions prohibit any significant yield of benzaldehyde. Yet, within the pH range of about 11 to about 13, especially about 12 to about 12.5, significant yields on the order of 75% or greater are achieved and benzaldehyde is recoverable in substantially pure form free of side reaction products. These results are considered to be unexpected especially at the high pHs of the reaction where it may have been expected that side reactions would have significantly lessened or prevented the yield for the desired product.

___

This may be the method I've been looking for.

[Edited on 28-8-2011 by MeSynth]

------------------------------------------------------------------

Again I took the liberty. Please correct anything wrong with the following.... :)


I dont think foaming should be a problem when done on a small scale like the one I'm about to describe. After doing the math this is what I came up with. This is the scale I would do it at.

4673766

A stir bar and 32.5 ml of cinnamaldehyde is added to a 500ml round bottom flask (I'm going to do it in a 3 necked 500ml RB 14/20) followed by 222.5 ml of DH2O followed by just enough sodium hydroxide to make the ph 12-12.5 (something like 1.386 grams). A reflux adaptor is then fitted to this flask. Attach another condencer to the top of the reflux condencer and set it up for distilation. The reflux adaptor is then flooded with ice cold water. The mixture is then heated on an oil bath to reflux at 105C. The reflux is to be held for one hour with carful monitoring of the ph (to monitor it I will use the free neck of the 3 necked rb flask) making sure to keep it within the range of 11 - 13. If the ph is starting to drop sodium hydroxide is added (this could be done by adding a drip or two of concentrated aqueous sodium hydroxide via addition funnle). After one hour the condencer set up for distillation is flooded with ice cold water. After it has cooled considerably the reflux condencers water supply is replaced with warm tap water and then left alone (or you can keep the waters temp set to 37.7 like the patent says) creating a temperature within the reflux condencer that will allow the water vapor to escape. The condencer set up for distilation will condence the vapor containing the benzaldehyde. As water leaves the mixture more water should be dripped in at the same rate it is leaving and the ph should still be monitored. This is not covered in the patent but I'm sure it is important.

The patent then distills the benzaldehyde under a vacuume that allows it to boil at 70C. This is done to separate it from the impurities. I'm sure this step could be skipped by doing a work up with sodium bisulfite.



[Edited on 28-8-2011 by MeSynth]

questions - 27-8-2011 at 20:38

Thanks guys, I really appreciate your thoughts on my questions :)

And it's good to see that we're all participating in helping one another, keep up the good work :)

questions - 30-8-2011 at 13:05

Hey guys

I was told by someone that the cannizaro reaction only happens when the solution is alkalai and this is when the ph is 14 plus. I'm confused because i'm thinking about a reaction that happens between the ph range of 12 to 13 to make benzaldehyde from cinnamon aldehyde as previously disscussed
.
Thus does the cannizaro reaction only happen at a ph of at least 14 or can it even happen at a range of say between 12 and 13 with aldehydes?

questions - 22-9-2011 at 02:24

I'm trying to find out at what PH the cannizarro reaction will happen at, does anyone know?

questions - 30-10-2011 at 22:27

Does anyone know what drip rate cyclonight used when he made benzaldehyde by slowly driping the cinnamon oil into the boiling mixture of water and NaOH.
That is, how many seconds between each drop of cinnamon ?

questions - 31-10-2011 at 01:06

Quote: Originally posted by CycloKnight  
Hi peeps, been off the forum a good while but its good to be back :).

I’ve significantly improved the original batch method I posted last year, what follows is my latest method.

This approach uses the same setup as the last steam distillation variation graphically depicted in in this thread.

Basically, the items used were:
hot plate, pressure cooker steam generator & associated tubing, etc
3L 3-neck RBF & mantle
vigreux column, right angle bend & still head
condenser
Vacuum pump & glassware for purfying the final product & recycling unreacted cinnamaldehyde.

chemicals: 2 litres tap water, lecithin, cinnamon oil, NaOH

Essentially, a large reaction vessel and a means of steam & vacuum distilling are all the equipment really required.


Begin by setting up all equipment, add 2 L water & ~1.5g lecithin.
The first variation is to use OTC sodium hydroxide instead of sodium carbonate, simply add the alkali to adjust the pH within the range of 12-13, only small amounts are required.

The second variation is to slowly drip in the cinnamon oil during the course of the reaction, the benzaldehyde being steam distilled as it forms. Begin the addition once the pH adjusted solution has heated to boling temperature and the steam is passing though the solution.

The third variation is to stop the cinnamon oil addition after 5 min, then check the distillate. If benzaldehyde is clearly distilling over, then continue with the addition.
A crude test is to simply taste the steam distillate as it drips into the receiving vessel, if it burns your tongue off, then you're doing well. If it tastes sweet, then significant quantities of cinnamon are being carried over. Should this not change after a short while, then double check the pH !

Provided that the pH is correct and the cinnamaldehyde content is high (70%+) then benzaldehyde laden distillate should start collecting almost immediately after the addition has begun.
However, if it is not, wait for the benzadehyde to start collecting, THEN continue with the addition. This prevents unnecessary amounts of cinnamaldehyde being steam distilled at the start of the process, which is a serious problem with the old batch mode reaction.

Note that by slowly dripping the cinnamon oil instead of adding it all at once to the reaction mix, single run conversion is increased by 20-30%.

Ensure the rate of cinnamon oil drip rate is approximately equivalent to the quantity of oil being steam distilled, thus maintaining high dilution in the reaction mixture.

After 300 to 500 ml of cinnamon oil had been added, the drip rate is stopped and the steam distillation continued until all the aldehyde has been steam distilled from the reaction mix. If using less than 2L of water, then adjust proportionally to maintain the same dilution. At this point, dump the mix and replace with clean pH adusted water with at least ~1.5g lecithin.
This step removes tar and other junk that slows down the reaction and reduces benzaldehyde production. Significantly reduced tar formation will also result from periodically carrying out this step (very imporant if high yields are desired).
Also note that with this method, the pH tends to slowly drop over time during the course of the steam distillation, so check the pH every couple hours, and top up with NaOH if and when required. Its preferable to simply add small amounts concentrated NaOH solution when topping up, using a dropper makes the alkali addition much simpler since NaOH pellets will rapidly collect moisture and stick to the sides of the reaction vessel.

Efficiency is further improved if the steam distillate (after oil separation) is also extracted with DCM, though this isn't absolutely necessary.

Once the the product oil is pooled, vacuum distillation will remove the benzaldehyde - no need to vacuum distill the recycle cinnamon aldehyde, just drip it into the steam distillation vessel, just as with the cinnamon oil feed. Expect the quantity of unreacted cinnamon aldehyde to be circa 25%, but if the reaction mix was kept clean during the process then it may be considerably less. The benzaldehyde distillate is clear, & much purer than the original solvent extraction method that doesn't employ the steam distillation. Give the batch solvent extraction a rest folks, use the steam distillation variation if producing benzaldehyde from cinnamon oil!
Far, far less work.

Using the above approach, overall molar conversion to benzdehyde is at least 80%.

I’ve managed higher conversion efficiencies (~90%), but the reaction efficiency is subject to variation according to varying reaction conditions, i.e. feed rate, reaction mix volume (i.e. dilution), and the quantity of cinnamon oil fed to the reaction mix before changing the solution. >80% seems to be a realistic overall figure.

Also...
Remember to keep the reaction mix free of tar & cinnamon oil impurities as much as possible to give consistent high yields.

If dripping the aldehyde into the mixture isn't practical for any reason, you can periodically add the cinnamon oil in small batches, say 20-50 ml at a time to give good conversion, but expect a little more cinnamonaldehyde to distill over.


OK everyone, I've given this alot of thought and now I need everyones help on this because I am not in a possition to do the experiment myself.

When cyclonight said that after the 300-500ml had finished dripping the cinnamon oil into the 2L of boiling water with NaOH in it, how long did it take for the whole 300-500ml to completely drip in because he never said what the drip rate was?

questions - 8-11-2011 at 17:47

does anyone know how long it took cyclonnight to drip the 300 to 400ml of cinnamon oil into the 2l of boiling water with naoh in it at ph 12to 13?

ANYONE?

ANYONE AT ALL?..........

Neil - 8-11-2011 at 17:56


Quote:

Ensure the rate of cinnamon oil drip rate is approximately equivalent to the quantity of oil being steam distilled, thus maintaining high dilution in the reaction mixture.



That long.

questions - 11-11-2011 at 04:19

OK Neil, I appreaciate your input put there are several factors that will affect how long it takes for the benzaldehyde/cinnamon disstillate to come over, some are;

1) the drip rate
2) the amount of steam that is blown into the solution
3) the presure of the steam as it goes into the solution

these ar the three crucial factors that cyclonights posts have ommited, and naturaly if you were to alter one/some/all of the three points i've mentioned above you will get different disstilation amounts and different conversion amounts into benzaldehdye.
I'm wanting to know that based on "cyclonights" conversions (circa 75%), how long did it take him to get te whole300ml to 500ml through the solution


watson.fawkes - 11-11-2011 at 06:29

Quote: Originally posted by questions  
1) the drip rate
2) the amount of steam that is blown into the solution
3) the presure of the steam as it goes into the solution
It sounds like you've got some good parameters for an experimental design. Please report what you find here. I'm sure others will appreciate it.

questions - 11-11-2011 at 07:08

doing that experiment would be the one thing i would love to do, but unfortunately I am living with my mum and dad and they dont like the idea of me doing stuff like that. Also I have not the equipment and location right now to do the experiment.
Thus, I'm just wanting to see if anyone else has done the experiment and can shed some light on it.

watson.fawkes - 11-11-2011 at 08:04

Quote: Originally posted by questions  
I am living with my mum and dad and they dont like the idea of me doing stuff like that. Also I have not the equipment and location right now to do the experiment.
So why do you care? If you can't do the experiment, you wouldn't be able to do the synthesis either.

questions - 11-11-2011 at 18:34

I'm only interested in knowing how it works for my own knowledge. I'm curious.

Also, what would happen if benzaldehyde made contact with aluminum?

Panache - 16-11-2011 at 01:26

Quote: Originally posted by questions  
I'm only interested in knowing how it works for my own knowledge. I'm curious.

Also, what would happen if benzaldehyde made contact with aluminum?


Depends on the temperature. I know fairly certainly that if the temperature of the aluminum is less than -150C, the benzaldehyde will likely freeze and nothing further will occur. If the aluminum is at 3000C or above the benzaldehyde will likely be destroyed quickly. Other than that I can't say for sure.
Hope this helps!

questions - 20-12-2011 at 02:04

There is no easy way to make benzaldehyde, I think the best way is to get it from a chemical company that use it for their business and try buying it from them.

I have tried most of the benzaldehyde making methods and they all yeild very little product.

questions - 23-12-2011 at 19:18

I cant do the experiment myself right now as I'm in the process of relocating but my situation is this;

I'm wanting to try cyclonights method that he explained on page six where he slowly dripped the cinnamon oil into the boiling solution of NaOH with a ph of around 12.6 and had steam blowing in at the same time to disstill the formed benzaldehyde.
The product he obtained was about 75% benzaldehyde and the other 25% was the unreacted cinnamon oil. He then took this product and vacuumed disstilled it to get pure benzaldehyde, very interesting method.

He doesnt state how many seconds that were between each drip of cinnamon as it dripped into the 2L boiling solution of water and NaOH and he doesnt state how long it took for the product to be completely distilled.

If I was to use the same amount of cinnamon oil that cyclonight used but instead of using 2L of boiling solution of water and NaOH like he used, say I used an 8L of solution instead, does that mean I would need four times as much steam pressure to get the same amount of product to disstill over?

Panache - 24-12-2011 at 02:26

Is there a reason people are so intrigued with methods other than toluene, uv, chlorine, then hydrolysis with hcl to benzaldehyde. Its reliable, scalable and safe, if you consider producing chlorotoluenes safe.

Also when i tried the method of dripping the cinnamon oil into the naoh i found it considerably superiorto bleed the cinnamon oil into the steam line, this created a massive dispersion of fine oily droplts.

Also don't try doing this in glass, it doesn't work reliably at those pressures.simply use two camping gas cylinders, one for generating the steam, the other for the reaction. Lead the outlet vapour into a glass condenser, downwards, a coiled jacketed one to handle the shitloads of steam one needs to condense, also did i mention this method is unreliable, inconsistent and a pain in the arse. :D

questions - 24-12-2011 at 03:25

Then how did cyclonight get such good results?

Panache - 24-12-2011 at 04:43

Do we know that? We know he said what he said, as did i, maybe he exaggerated, maybe i downplayed it, maybe i exaggerated and he downplayed it. Sm is not peer reviewed. Maybe instead of benzaldehyde i'm getting mad kilo's of gold out of the reaction and i'm greedy and want no one else to know.

Maybe he had accepted jesus as his lord and saviour and was blessed by the wholely (or is that holely) spirit.

Maybe his raiki was tuned better into his chakras.

Maybe you should tell your parents to jam it and do an experiment.

One things for certain,

WE WILL NEVER KNOW.

questions - 24-12-2011 at 05:09

very funny lol :)

simba - 24-12-2011 at 07:00

Quote: Originally posted by questions  
There is no easy way to make benzaldehyde, I think the best way is to get it from a chemical company that use it for their business and try buying it from them.

I have tried most of the benzaldehyde making methods and they all yeild very little product.


Indeed. I managed to buy piperonal this way.

questions - 24-12-2011 at 17:29

Has anybody else actually tried cyclonights cinnamon oil method of making benzaldehyde by slowly dripping the oil into the reaction mix and steam disstilling the formed benzaldehyde at the sae time?

peach - 24-12-2011 at 18:21

I have, but I preferred the persulphate method.

questions - 24-12-2011 at 18:32

was the coversion rate of cinnamon oil to benzaldehyde really like around 75% to 90% like he says?

And how long dd it take to drip all the cinnamon oil through and how much cinnamon oil did you use?

questions - 24-12-2011 at 18:35

Quote: Originally posted by peach  
I have, but I preferred the persulphate method.


was the conversion rate of cinnamon oil to benzaldehyde really like 75% to 90% like cyclonight said?

Also, how much cinnamon oil did you drip into the reaction mix and how long did it take for all the cinnamon to drip in?

you can see how facinated i am by this method :)

Cinnamon oil to benzaldehyde

questions - 24-12-2011 at 20:25

OK everyone, there has been a lot of hype about making benzaldehyde from tolune. I personaly believe that it may be easier to make benzaldehyde from cinamon oil that has a high content of cinnamon aldehyde as it has been illustrated by an old user called cyclonight. Unfortunately cyclonight hasn't been on this site for like ages and I have read his work and have accumulated a lot of questions which I'm trying to find answers to.
I am not in a position to do an experiment as I'm living with my parants and they hate the idea of me playing around with this stuff and we're now in the process of moving.
Thus every time I ask questions about making benzaldehyde from cinamon everyone gets annoid for they areonly intereste in making benzaldehyde from toluene, which I have personaly done and have found that process an incredably huge waste of time. I would have theee hot plate stirrers and three 500ml beackers on each and it would take hours to charge the solution with electricity up and then it would take about anoter hour to convert the toluene to benzaldehyde and the yeildswere very lown and then I would have to disstil the benzaldehyde out under vacuum and after spending a whole week wrth of work, i'd only have about 50ml to 75ml of pure benzaldehyde. It really wasn't worth the effort.
I have since been trying to find more people who are interested in finding amethod that can be used to makelarge quantities of benzaldehyde and I believe there is some hope in the cinnamon oil method. Thats right, that very common and cheap cinnamon oil you buy over the counter in any health food store or even over the internt, that is what is used to make benzaldehyde.
I will provide the link that cyclonight posted and hopefuly we can all pool our experience and knowledg and master the method of making benzaldehyde from ccinnamon oil (cassia oil).

questions - 24-12-2011 at 20:31

OK everyone, here is the method discovered by cyclonight, apparently this is the bees kness for making benzaldehyde according to cyclonight who has proven himself to be a very smart and credable person who likes to experiment.

This is what we need to experiment with and work on and hopefully even improve;


Cinnamon oil to benzaldehyde update.


Hi peeps, been off the forum a good while but its good to be back .

I’ve significantly improved the original batch method I posted last year, what follows is my latest method.

This approach uses the same setup as the last steam distillation variation graphically depicted in in this thread.

Basically, the items used were:
hot plate, pressure cooker steam generator & associated tubing, etc
3L 3-neck RBF & mantle
vigreux column, right angle bend & still head
condenser
Vacuum pump & glassware for purfying the final product & recycling unreacted cinnamaldehyde.

chemicals: 2 litres tap water, lecithin, cinnamon oil, NaOH

Essentially, a large reaction vessel and a means of steam & vacuum distilling are all the equipment really required.


Begin by setting up all equipment, add 2 L water & ~1.5g lecithin.
The first variation is to use OTC sodium hydroxide instead of sodium carbonate, simply add the alkali to adjust the pH within the range of 12-13, only small amounts are required.

The second variation is to slowly drip in the cinnamon oil during the course of the reaction, the benzaldehyde being steam distilled as it forms. Begin the addition once the pH adjusted solution has heated to boling temperature and the steam is passing though the solution.

The third variation is to stop the cinnamon oil addition after 5 min, then check the distillate. If benzaldehyde is clearly distilling over, then continue with the addition.
A crude test is to simply taste the steam distillate as it drips into the receiving vessel, if it burns your tongue off, then you're doing well. If it tastes sweet, then significant quantities of cinnamon are being carried over. Should this not change after a short while, then double check the pH !

Provided that the pH is correct and the cinnamaldehyde content is high (70%+) then benzaldehyde laden distillate should start collecting almost immediately after the addition has begun.
However, if it is not, wait for the benzadehyde to start collecting, THEN continue with the addition. This prevents unnecessary amounts of cinnamaldehyde being steam distilled at the start of the process, which is a serious problem with the old batch mode reaction.

Note that by slowly dripping the cinnamon oil instead of adding it all at once to the reaction mix, single run conversion is increased by 20-30%.

Ensure the rate of cinnamon oil drip rate is approximately equivalent to the quantity of oil being steam distilled, thus maintaining high dilution in the reaction mixture.

After 300 to 500 ml of cinnamon oil had been added, the drip rate is stopped and the steam distillation continued until all the aldehyde has been steam distilled from the reaction mix. If using less than 2L of water, then adjust proportionally to maintain the same dilution. At this point, dump the mix and replace with clean pH adusted water with at least ~1.5g lecithin.
This step removes tar and other junk that slows down the reaction and reduces benzaldehyde production. Significantly reduced tar formation will also result from periodically carrying out this step (very imporant if high yields are desired).
Also note that with this method, the pH tends to slowly drop over time during the course of the steam distillation, so check the pH every couple hours, and top up with NaOH if and when required. Its preferable to simply add small amounts concentrated NaOH solution when topping up, using a dropper makes the alkali addition much simpler since NaOH pellets will rapidly collect moisture and stick to the sides of the reaction vessel.

Efficiency is further improved if the steam distillate (after oil separation) is also extracted with DCM, though this isn't absolutely necessary.

Once the the product oil is pooled, vacuum distillation will remove the benzaldehyde - no need to vacuum distill the recycle cinnamon aldehyde, just drip it into the steam distillation vessel, just as with the cinnamon oil feed. Expect the quantity of unreacted cinnamon aldehyde to be circa 25%, but if the reaction mix was kept clean during the process then it may be considerably less. The benzaldehyde distillate is clear, & much purer than the original solvent extraction method that doesn't employ the steam distillation. Give the batch solvent extraction a rest folks, use the steam distillation variation if producing benzaldehyde from cinnamon oil!
Far, far less work.

Using the above approach, overall molar conversion to benzdehyde is at least 80%.

I’ve managed higher conversion efficiencies (~90%), but the reaction efficiency is subject to variation according to varying reaction conditions, i.e. feed rate, reaction mix volume (i.e. dilution), and the quantity of cinnamon oil fed to the reaction mix before changing the solution. >80% seems to be a realistic overall figure.

Also...
Remember to keep the reaction mix free of tar & cinnamon oil impurities as much as possible to give consistent high yields.

If dripping the aldehyde into the mixture isn't practical for any reason, you can periodically add the cinnamon oil in small batches, say 20-50 ml at a time to give good conversion, but expect a little more cinnamonaldehyde to distill over.

questions - 24-12-2011 at 20:34

OK guys, I have made a thread for making benzaldehyde from cinnamon oil. Clearly you are tunnel visioned by making benzaldehyde from toluene (and good luck to you), but for those of you who have an interest in this new and not so talked about method whereby cinnamon is used, then come to this new thead and share your ideas :)

The thread is called; cinnamon oil to benzaldehyde

http://www.sciencemadness.org/talk/viewthread.php?tid=18351#...

entropy51 - 24-12-2011 at 20:44

Quote: Originally posted by questions  
I have tried most of the benzaldehyde making methods and they all yeild very little product.
Then you're doing it wrong. As in the way you misspelled "yield".
Quote: Originally posted by questions  
My lab was at my friends house and we did our little experiments in his garage. Unfortunately his mother has found a new guy and he is now living in the house and has started asking questions about us. I cant experiment in there anymore and it would be far too difficult for me to do it anywhere else. Also, I'm still living at home with my parents and they'd kill me if they sore me doing those sort of things :(
Thus I'm hoping to find people who have already done these things and can help me out, it sucks I know :(
Oh, now I understand why.

[Edited on 25-12-2011 by entropy51]

questions - 24-12-2011 at 22:44

Making benzalehyde via oxidisng toluene is the method tha was using and I would only get 50ml to about 75ml per time.
would have o spend hours charging he cell up and then more time to convert the cinamon to benzaldehyde. The process was very corosive as ev erythingin the garagethat was made of steel was corroding, even the screws in the door that hold the know to the door were corroded out.
Using the toluene method isthe hardest method possible it sucks.
Not just that but it is very time consuming to remove all the benzaldehyde, toluene and byproducts out of the mix after i has been discharged in the reaction.

Overall I can tell you from 6 months ofsolid practise off this method that it sucks arse




questions - 24-12-2011 at 22:47

It sucks arse because of four main reasons;

1) It is corrosive to things around it

2) It uses up too many reasorces

3) The reaction takes to long to complete

4) The produt obtained is very little given the large amount of work involved

questions - 5-1-2012 at 05:06

I managed to do my first experiment in converting the cinnamon oil to benzaldehyde at my mates house while his mum went to queensland :)

basically we added 200 ml of cinnamon oil to 2L of boiling water with NaOH in it at ph of about 12.88 and boiled it for 7 hours n a round bottom flask. The reaction went for seven hours and it was then that we ecided to stop the reaction and see the yeilds and much to our dissmay, we found that about 60% of the cinamon oil had turned to tar, the other 30% had turned into benzaldehyde and the other 10% was unreacted cinnamon oil.

I have discovered that there is basically one thing wrong with this reacion that is making it such a pain in the arse for everyone.
Basically as the cinnamon aldehyde turns into benzaldehyde, the benzaldehyde emediatly starts to turn into tar and sludge-like-shit.
The problem here is that we need a way to preserve the formed benzaldehyde as it remains in the solution as it is formed so to stop it from turning into shit after it has been made from the cinnamon aldehyde.

Do you have any such ideas that would help minimise the benzaldehyde from turning into tar durring the course of the reaction?

questions - 6-1-2012 at 07:53

I love benzaldehyde, not just for it's broad uses, but because of it's signature smell and oily texture, it's also very xpensive as well I hear.

I've been doing a lot of research into the reaction of cinnamon aldehyde in a boiling solution of water with ph 11 to 13 and antifoaming agent.
I've tried the experiment and have found that the more benzaldehyde is made, the more tar is formed in the reaction.
After an 7 hour reaction of 200ml of cinnamon aldehyde in a 2L solution of boling water with a steady ph of 12.5 and antifoaming agent, only 30% was benzaldehyde, 20% was unreacted cinnamon and the other 50% was all this tar shit.

I think that the aceteldehyde is reacting with the benzaldehyde in this base solution and that is what is making all this tar shit. Because I don't believe that this tar shit is a product of the cinnamon turning into benzaldehyde and acetaldehyde, I think that shortly after the benzaldehyde has formed, it reacts with the acetaldehyde that has formed. I cant think of any other explanation and I certainly dont think that the benzaldehyde is reacting with the cinnamon, could it????

If it is such that the formed benzaldehyde is reacting with the formed acetaldehyde, what can we put in place to stop or even minimise this from happening?

questions - 6-1-2012 at 08:23

Yep, the acetaldehyde is definately reacting with the presious benzaldehyde thats fored in the reaction with cinnamon oil in boiling water with ph 12 as illustrated in point 2)

http://web.pdx.edu/~wamserc/CH332W97/homework/H11ans.htm

jsc - 17-1-2012 at 09:59

What are you, some kind of almond freak?

Why can't you be a normal kid and make explosives?