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Syn the Sizer
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Exactly, the suggested solvents are easy to get, aluminum is no problem to get as is bromine and the aluminum can be doped with a copper salt, doesn't
need to be mercury chloride.
here is a video too shared with me a while back.
https://youtu.be/6Uv1NbaITYM
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Texium
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Quote: Originally posted by Benignium  | I read about piperonal turning brown on light exposure on PubChem and always just assumed that the same phenomenon affected my sample, but now I question this. Perhaps once again it's due to impurity.
Luckily there is a way to find out.
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The piperonal we had in the research lab was stored at room temperature without any apparent deterioration
and looked like light cream colored crystals. And yes, it smelled heavenly. I would describe it as cherry-vanilla but with more depth.
[Edited on 2-28-2021 by Texium (zts16)]
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arkoma
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@syn--example 2 is activated with copper, and the reaction solvent is xylene. Very doable demethylation, and i've seen the vid you referenced and
forgot all about it.
"We believe the knowledge and cultural heritage of mankind should be accessible to all people around the world, regardless of their wealth, social
status, nationality, citizenship, etc" z-lib
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zed
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Well, the reaction conditions produced something. Exactly what, is not proven. So, maybe it worked.
As for Heliotropine and Pyridine.... Heaven and Hell?
I haven't had a whiff of Pyridine in ages. God, what a stink! You never forget it.
As for Heliotropine, you can smell it easily enough, in microscopic quantities.
It's not Quite the same, but Piperonal is called Heliotropin, after the flower.
Nice smelling flower it is.
https://www.ilonasgarden.com/heliotrope/
[Edited on 28-2-2021 by zed]
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Syn the Sizer
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| Quote: Originally posted by arkoma | | @syn--example 2 is activated with copper, and the reaction solvent is xylene. Very doable demethylation, and i've seen the vid you referenced and
forgot all about it. |
exactly, my thoughts too.
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karlos³
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I put a few milligrams of piperonal in my vaping fluid(tobacco scented), it goes along pretty great together with the aromatic virginia tobacco!
Mhmmm... I guess it doubled my daily nicotine dose though 
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draculic acid69
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| Quote: Originally posted by DraconicAcid | | Quote: Originally posted by Benignium | DraconicAcid - Which ones are you interested in and why, if you don't mind me asking? I checked out a few at random and the acetic
acid ester for one sounds like it would make a fantastic addition to a collection of aroma compounds!
|
Just for smells- methyl and ethyl piperonylate should be nice. Methyl and ethyl piperonate, too (but my hydrolysis of piperine didn't give a very
high yield of the acid, so I haven't tried that yet). |
Also of interest to those desiring these things for the interesting smells I've seen
that the mdPhMeCOOH is widely available off Alibaba. It should also make some
very interesting smelling esters.
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Benignium
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Thank you, Syn the Sizer, for bringing up this approach. I did actually see this video while planning for the reaction but have since forgotten all
about it.
I think I'll try that next since I already have all the necessary reagents, and save the pyridine for something different.
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DraconicAcid
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| Quote: Originally posted by draculic acid69 | | Quote: Originally posted by DraconicAcid | | Quote: Originally posted by Benignium | DraconicAcid - Which ones are you interested in and why, if you don't mind me asking? I checked out a few at random and the acetic
acid ester for one sounds like it would make a fantastic addition to a collection of aroma compounds!
|
Just for smells- methyl and ethyl piperonylate should be nice. Methyl and ethyl piperonate, too (but my hydrolysis of piperine didn't give a very
high yield of the acid, so I haven't tried that yet). |
Also of interest to those desiring these things for the interesting smells I've seen
that the mdPhMeCOOH is widely available off Alibaba. It should also make some
very interesting smelling esters.
|
Is that phenylacetic acid? I made a small amount of that a year or so ago, but didn't turn it into an ester (yet). I'd also like to find an easy way
to turn cinnamic aicd into hydrocinnamic acid......
[Edited on 1-3-2021 by DraconicAcid]
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
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Benignium
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Homopiperonylic acid, I believe:
https://www.sigmaaldrich.com/catalog/product/aldrich/329673?...
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DraconicAcid
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Ah, that makes sense. And yes, Alibaba has it for $10/kg ($6/kg if you're buying more than 100 kg at once).
I may get the college to start ordering all the chemicals I want to play with from there....
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
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Syn the Sizer
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| Quote: Originally posted by karlos³ | I put a few milligrams of piperonal in my vaping fluid(tobacco scented), it goes along pretty great together with the aromatic virginia tobacco!
Mhmmm... I guess it doubled my daily nicotine dose though
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Interesting, I am curious about the taste as well.
| Quote: Originally posted by draculic acid69 |
Also of interest to those desiring these things for the interesting smells I've seen
that the mdPhMeCOOH is widely available off Alibaba. It should also make some
very interesting smelling esters.
|
Yes, I had heard about that, but I forgot they had it, thanks man.
| Quote: Originally posted by Benignium | Thank you, Syn the Sizer, for bringing up this approach. I did actually see this video while planning for the reaction but have since forgotten all
about it.
I think I'll try that next since I already have all the necessary reagents, and save the pyridine for something different.
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Np man, I knew I had it but didn't think to mention it until I got home and found the paper.
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DraconicAcid
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(As an aside, how is Alibaba for buying small quantities? Such as shipping rates? I've only used AliExpress.)
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
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draculic acid69
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| Quote: Originally posted by DraconicAcid | | Quote: Originally posted by draculic acid69 | | Quote: Originally posted by DraconicAcid | | Quote: Originally posted by Benignium | DraconicAcid - Which ones are you interested in and why, if you don't mind me asking? I checked out a few at random and the acetic
acid ester for one sounds like it would make a fantastic addition to a collection of aroma compounds!
|
Just for smells- methyl and ethyl piperonylate should be nice. Methyl and ethyl piperonate, too (but my hydrolysis of piperine didn't give a very
high yield of the acid, so I haven't tried that yet). |
Also of interest to those desiring these things for the interesting smells I've seen
that the mdPhMeCOOH is widely available off Alibaba. It should also make some
very interesting smelling esters.
|
Is that phenylacetic acid? I made a small amount of that a year or so ago, but didn't turn it into an ester (yet). I'd also like to find an easy way
to turn cinnamic aicd into hydrocinnamic acid......
[Edited on 1-3-2021 by DraconicAcid] |
Yes it's the mdphenylacetic.
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draculic acid69
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No idea.ive only bought plastic resins off Alibaba. I'd recommend AliExpress if possible as my experience was slow and not painless. Experience with
AliExpress was way smoother
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njl
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It's not too bad, personally I take a lot of time when looking for supplies because pricing is always a mystery. You can get good deals for small
quantities, but you may still end up paying twice that for shipping (real example: 50 grams/60 USD + 100 USD shipping). Because most of the listed
prices are not accurate, you will have to speak to the supplier anyway and may as well ask for a sample quantity or just a smaller order. Many will
work with you. It really depends on what you're looking for too, and how you present yourself when speaking with suppliers.
Reflux condenser?? I barely know her!
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Syn the Sizer
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I have heard with Alibaba the best thing to do is contact several sellers for pricing. Some may send samples as well. Find the best pricing and let
the other sellers know you found a better price and they sometimes lower their prices to get you business, same as dropping quantities.
Some may have a min order of 10Kg and another 500g but a higher price, so they may drop down to 1000g for the same price. This example is just
speculation but when a seller is buying 100Kg+ for a great price, they sometimes really work with you.
I have had non Alibaba sellers change quantities and whatnot to keep my business.
I have no first hand experience, this is just a word of mouth thing from others who have ordered.
Syn'
[Edited on 2-3-2021 by Syn the Sizer]
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Mateo_swe
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OrgSyn describes a electric reduction method that seem quite easy for making hydrocinnamic acid from cinnamic acid.
The porous cup can be an unglazed clay flowerpot if you can find one without hole in the bottom.
Look at Orgsyn, Collective Volume, 1, p. 311.
Or view the PDF
Attachment: Hydrocinnamic acid - Orgsyn.pdf (316kB)
This file has been downloaded 532 times
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karlos³
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If you buy a quantity below a kilo(usually), you will probably pay still almost the same price.
Usually it only pays off if you buy a kilogram at least, which is standard there for almost every chemical.
Otherwise you will face prices like for 100g 3/4th of the price of a whole kilo and such.
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clearly_not_atara
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| Quote: Originally posted by Syn the Sizer | I finally got the time to actually find the patent.
This demonstrates a method of demethylating vanillin using aluminum bromide produced in situ from elemental bromine and elemental aluminum in an
variety of aryl solvents. They boast a ~90% yield.
They explain the advantages over other methods. |
Everything old is new again:
http://www.sciencemadness.org/talk/viewthread.php?tid=92847&...
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DraconicAcid
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| Quote: Originally posted by Mateo_swe |
OrgSyn describes a electric reduction method that seem quite easy for making hydrocinnamic acid from cinnamic acid.
The porous cup can be an unglazed clay flowerpot if you can find one without hole in the bottom.
Look at Orgsyn, Collective Volume, 1, p. 311.
Or view the PDF |
Yes, I know that method, but mucking around with a mercury electrode doesn't fit my definition of easy. Thanks anyway.
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
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AvBaeyer
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DraconicAcid,
If you have nickel chloride and zinc dust at hand, your desired reduction will proceed quite nicely. I have been doing several of the cinnamate
reductions recently and they work very well if you do not mind a bit of inorganic waste. I have been using the procedure in
Nose and Kudo, Chem. Pharm. Bull. Japan, 38, 2097 (1990).
I have been running the reactions on a 10 mmole scale using the procedures described in the paper. My isolated yields are all >90% and the
reduction is complete based on the permanganate spot test of the isolated products. I prefer reducing the cinnamate methyl esters as the work up is
more convenient.
This is not the most "modern" of reductions but it works, reagents are readily available and it is easily adaptable to the hobby lab.
Hope this helps.
AvB
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myr
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| Quote: Originally posted by AvBaeyer | DraconicAcid,
If you have nickel chloride and zinc dust at hand, your desired reduction will proceed quite nicely. I have been doing several of the cinnamate
reductions recently and they work very well if you do not mind a bit of inorganic waste. I have been using the procedure in
Nose and Kudo, Chem. Pharm. Bull. Japan, 38, 2097 (1990).
I have been running the reactions on a 10 mmole scale using the procedures described in the paper. My isolated yields are all >90% and the
reduction is complete based on the permanganate spot test of the isolated products. I prefer reducing the cinnamate methyl esters as the work up is
more convenient.
This is not the most "modern" of reductions but it works, reagents are readily available and it is easily adaptable to the hobby lab.
Hope this helps.
AvB |
Some papers also claim Cu/Zn couple can also achieve the same reduction in good yield: DOI:10.1039/P19830001219 . I also remember something ab a
dithionite system working too, but I cant seem to find the relevant paper.
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