| Pages:
1
2 |
Hexavalent
International Hazard
Posts: 1564
Registered: 29-12-2011
Location: Wales, UK
Member Is Offline
Mood: Pericyclic
|
|
New Amateur Way to Prepare Pyridine
Here is a new idea I've had for the preparation of pyridine by the amateur, which came partially from Magpie's original idea and this paper.
It simply involves the reaction of pyridine-3-carboxylic acid, or niacin/nicotinic acid, with a soluble copper salt to produce the transition metal
complex copper (II) nicotinate, and then the thermal decomposition of this under a distillation setup to collect the pyridine which forms and
evaporates at the high temperatures.
Any suggestions or ideas for development with this?
Magpie's original work was undeniably excellent, but this is intended to be an alternative for those who don't have access to the salts specified for
the catalyst he uses or the silver salts suggested by another user in his thread.
[Edited on 18-5-2012 by Hexavalent]
"Success is going from failure to failure without loss of enthusiasm." Winston Churchill
|
|
|
jon
Hazard to Others
Posts: 459
Registered: 11-1-2006
Member Is Offline
Mood: paranoid distrustful apprehensive
|
|
antocho the russian chemist at the hive got it right using 1/3 naoh CAO
just heated to about 320 until the pyridine distilled off it was used for qauntitative analysis so i'm sure it yeilded well
Give me librium or give me meth!
Patrick Henry....
|
|
|
Hexavalent
International Hazard
Posts: 1564
Registered: 29-12-2011
Location: Wales, UK
Member Is Offline
Mood: Pericyclic
|
|
Can you please word your answer slightly better? Got what right? Do you mean the thermal decomposition?
What do you mean by 1/3 NaOH (and do you also mean CaO)? Writing formulae correctly really helps other people interpret your suggestions and answers.
According to what I've read, both in the paper and what I was told by Polverone, no additional solids are needed, just to heat the copper complex in a
distillation rig is sufficient. I could perhaps understand why Ca(OH)2 could be added, perhaps to absorb some of the CO2, but that's as far as I can
understand with what you've written so far.
[Edited on 18-5-2012 by Hexavalent]
"Success is going from failure to failure without loss of enthusiasm." Winston Churchill
|
|
|
Nicodem
Super Moderator
Posts: 4230
Registered: 28-12-2004
Member Is Offline
Mood: No Mood
|
|
Usually it's not worth bothering with jon's dementia, but he is probably trying to derange the discussion to a different type of decarboxylation that
has nothing to do with the Cu-catalysed one. The possibility of that type of decarboxylation on nicotinic acid was already suggested in some posts in
the Pyridine synthesis/extraction thread. I don't remember ever reading Antoncho's report on this type of decarboxylation and currently don't have the
time to search the Hyperlab forum or the old Hive's remains, but you can ask Antoncho directly. He has an member account here, or alternatively ask
him at the Hyperlab in case he rarely checks his U2U messages here.
I would suggest you to follow the exact procedure that Magpie did, but substitute copper chromite with anything from 1/2 to an equal amount of basic
copper carbonate (CuCO<sub>3</sub>.Cu(OH)<sub>2</sub> . This
can easily be prepared from copper(II) sulfate. I'm sure there must be examples of its preparation on the forum, or at least references toward it. It
is worth trying, as even if it does not work it is still a scientific contribution.
…there is a human touch of the cultist “believer” in every theorist that he must struggle against as being
unworthy of the scientist. Some of the greatest men of science have publicly repudiated a theory which earlier they hotly defended. In this lies their
scientific temper, not in the scientific defense of the theory. - Weston La Barre (Ghost Dance, 1972)
Read the The ScienceMadness Guidelines!
|
|
|
Hexavalent
International Hazard
Posts: 1564
Registered: 29-12-2011
Location: Wales, UK
Member Is Offline
Mood: Pericyclic
|
|
Thanks for the idea, Nicodem. I'll ppt. some fresh basic copper carbonate and dry it later and have a go, following Magpie's procedure.
Would you recommend a half-to-full MOLAR or MASS amount if substituting basic copper carbonate for the chromite?
[Edited on 19-5-2012 by Hexavalent]
"Success is going from failure to failure without loss of enthusiasm." Winston Churchill
|
|
|
Nicodem
Super Moderator
Posts: 4230
Registered: 28-12-2004
Member Is Offline
Mood: No Mood
|
|
Well, empirical conversion and selectivity measurements are the only way to find out the optimal catalyst loadings. There is no way to calculate such
things. Magpie used about 11 mol% of the catalyst and it worked fine for his reaction conditions. So I would suggest to try out with anything from 5
to 20 mol% of CuCO3.Cu(OH)2.
The concept of "amount" in chemistry means amounts of substances measured in mol units (and not mass which is measured in grams): http://en.wikipedia.org/wiki/Amount_of_substance
This is because only amounts correlate in equivalents, while mass never correlates except in the case of isomers or simply coincidence.
…there is a human touch of the cultist “believer” in every theorist that he must struggle against as being
unworthy of the scientist. Some of the greatest men of science have publicly repudiated a theory which earlier they hotly defended. In this lies their
scientific temper, not in the scientific defense of the theory. - Weston La Barre (Ghost Dance, 1972)
Read the The ScienceMadness Guidelines!
|
|
|
GreenD
National Hazard
Posts: 623
Registered: 30-3-2011
Member Is Offline
Mood: Not really high anymore
|
|
I'm confused.
This isn't a catalyst, is it, as the carbonate gets used up, or is the carbonate regenerated by the loss of CO2 from the decarboxylation?
Why does copper carbonate work here, while copper nitrate wouldn't?
This may seem quite elementary but I am very young in understanding metallic catalysis.
ʃ Ψ*Ψ
Keepin' it real.
Check out my new collaborated site: MNMLimpact.com
|
|
|
Dr.Bob
International Hazard
Posts: 2734
Registered: 26-1-2011
Location: USA - NC
Member Is Offline
Mood: No Mood
|
|
If the copper is catalytic, then the proton from the original acid (or another nearby acid molecule) will protonate the cation generated by the loss
of CO2 from the carboxylate copper salt, and form the pyridine, at that point the copper is still oxidized and can react with another molecule of
acid. So the copper is not being reduced by the pyridine reaction, lose of CO2 leaves pyridine and CO2, which are both uncharged, so there is no net
reduction. The pyridine may complex with the pyridine formed, but that will break apart as the pyridine distills off.
And if there were some reduction of Cu(II), copper(0) at 280C would likely oxidize in air.
|
|
|
Nicodem
Super Moderator
Posts: 4230
Registered: 28-12-2004
Member Is Offline
Mood: No Mood
|
|
Quote: Originally posted by Dr.Bob  | | If the copper is catalytic, then the proton from the original acid (or another nearby acid molecule) will protonate the cation generated by the loss
of CO2 from the carboxylate copper salt, and form the pyridine, at that point the copper is still oxidized and can react with another molecule of
acid. |
The formation of an arylic carbocation is the least likely scenario from the thermodinamic perspective. Also, protons obviously do not protonate
cations as cations are generally acids.
There has been some moderate investigation into this reaction mechanism. A very good starting article and a must read for those getting involved in
this field of synthesis is DOI: 10.1021/ja00713a047. It also gives a good review of the older investigations.
According to the current understanding, the copper carboxylate losses CO2 to give the corresponding organocopper compound (hence the need for
efficient ligands). The ligand stabilized aryl-Cu intermediate then gets protodemetalated by another arylcarboxylic acid and the cycle continues again
and again (DOI: 10.1039/C1DT10771B). This mechanistic hypothesis explains all the experimental observations, including also the formation of biaryl
side products.
| Quote: | | So the copper is not being reduced by the pyridine reaction, lose of CO2 leaves pyridine and CO2, which are both uncharged, so there is no net
reduction. |
The Cu oxidation state in the precatalyst is of little importance. It was proved by ESR that the Cu(II) species get reduced to Cu(I) early in the
reaction when quinoline is used as the solvent. I would tend to believe such is the case in other media as well. In any case Cu is well known for its
ease of disproportionation reactions. Still, the use of inert atmosphere is recommended for these type of decarboxylations.
| Quote: Originally posted by GreenD | I'm confused.
This isn't a catalyst, is it, as the carbonate gets used up, or is the carbonate regenerated by the loss of CO2 from the decarboxylation?
Why does copper carbonate work here, while copper nitrate wouldn't? |
The correct terminology would be calling it a precatalyst, but since in organic synthesis a large proportion of all catalytic systems are actually
started by the use of a precatalyst, the use of this terminology kind of lost its value.
Copper nitrate is unlikely to work eficiently for several reasons. One of them is its acidity which would inhibit the likely required deprotonation of
the substrate. The other problem is the nitrate induced redox side reactions that would inhibit the formation of suitable amounts of active Cu(I)
species or decompose the reaction intermediates. Optimally, one designs experiments by using conditions that are most likely efficient according to
the reaction theory. The whole point of scientific investigations of the reaction mechanisms is the value these studies represent for the synthetic
chemists.
…there is a human touch of the cultist “believer” in every theorist that he must struggle against as being
unworthy of the scientist. Some of the greatest men of science have publicly repudiated a theory which earlier they hotly defended. In this lies their
scientific temper, not in the scientific defense of the theory. - Weston La Barre (Ghost Dance, 1972)
Read the The ScienceMadness Guidelines!
|
|
|
smaerd
International Hazard
Posts: 1262
Registered: 23-1-2010
Member Is Offline
Mood: hmm...
|
|
I've been very interested in copper ligands for decarboxylation on other substrates for a little while. Copper(II) Acetate can be made very easily as
well. In some cases a ligand will form using Copper Sulfate if one is patient.
Some of these ligands are not soluble in water or most other solvents aside from DMSO(even then sparingly). However I was given advice from a friend
that adding sulfuric acid to an insoluble ligand will allow them to be soluble in aq. solutions. Whereas with ammonium ion there was no notable
increase in solubility(iirc). On treatment with base the insoluble ligand forms again. I am not seasoned enough with metal-organic/inorganic chemistry
to know exactly how the sulfuric acid interacts here or if it actually destroys the complex or not. I'd like to know though.
An idea I have given only preliminary experiments towards was anodic oxidative decarboxylation of the sulfuric acid solutions, using Al electrodes. In
a single cell an electro-plating effect was noted on the Anode(brown thin 'rusty' layer formed on the side facing the other electrode maybe Cu(I)O?).
After basification an oily layer was observed which was not characteristic of the original solution. Again this was on another substrate, but it could
be worth further experimentation?
Thanks for the DOI reference nicodem, looks like a great place to start.
[Edited on 27-5-2012 by smaerd]
|
|
|
ubungy
Harmless
Posts: 3
Registered: 13-1-2011
Member Is Offline
Mood: No Mood
|
|
I ran the reaction of niacin with CuCO3.Cu(OH)2 in place of the copper chromite catalyst as per the directions in Magpie's thread, and recommendations in this thread. I hope it is okay to share my results here.
The niacin was obtained from GNC niacin supplement tablets (500mg) and recrystallized. Basic copper carbonate was precipitated from CuSO4 and Na2CO3.
For 8g niacin, I calculated 12.5 mol % CuCO3.Cu(OH)2:
8g/(123.11g/mol)=.065mol(.125)(221.12g/mol)=1.8g CuCO3.Cu(OH)2
Magpie's procedure was followed, substituting an oil bath for mantle. Oil temp was 160C when the rxn was started and immediately some water began to
form around the neck. The temperature was allowed to increase steadily, and at approx 235C the smell of pyridine was evident. (I was removing therm.
adapter for intermittent whiffs ) The temperature inside the still head reached
103C and decreased to 95C. 3.8ml of azeotropic mixture was collected, for approx 73% yield, assuming theoretical yield of 5.2ml.
Taking a mp of the recrystallized niacin indicated some impurity, probably the 'rice powder' from the supplements in the form of starch, as noticable
decomposition occured around 215-220C and some melting around 227C, below the literature value of 237C. I believe a better yield could be had from
purer niacin.
Also, if the water formed was from decomp of Cu(OH)2 (at 80C according to wikipedia), is there any reason the CuCO3.Cu(OH)2 just couldn't be dried at
120C or something prior to use?
Anyway, hope it was ok to post this, none of this was my idea I just ran the reaction. Also, it's been a year and a half, need an excuse to get my
first post out of the way  .
[Edited on 2-6-2012 by ubungy]
|
|
|
Hexavalent
International Hazard
Posts: 1564
Registered: 29-12-2011
Location: Wales, UK
Member Is Offline
Mood: Pericyclic
|
|
Very nice work ubungy, and an excellent first post. Congratulations!
What solvent did you use for the niacin recrystalliztion?
"Success is going from failure to failure without loss of enthusiasm." Winston Churchill
|
|
|
ubungy
Harmless
Posts: 3
Registered: 13-1-2011
Member Is Offline
Mood: No Mood
|
|
I used water for the recrystallization because I was low on ethanol. The tablets are 800mg containing 500mg niacin and I was able to remove a large
amount of insoluble material, but this wasn't the best option. There is solubility data on page 4 here.
I just went the other way though and am waiting for some usp grade from ebay.
|
|
|
Hexavalent
International Hazard
Posts: 1564
Registered: 29-12-2011
Location: Wales, UK
Member Is Offline
Mood: Pericyclic
|
|
Thanks a lot for that reference . . .it's difficult to find proper solubility curves and data for some compounds. I've plotted a graph of the data
you've given in that reference and drawn it up for a permanent record in my notebook for future reference.
"Success is going from failure to failure without loss of enthusiasm." Winston Churchill
|
|
|
SM2
Hazard to Others
Posts: 359
Registered: 8-5-2012
Location: the Irish Springs
Member Is Offline
Mood: Affect
|
|
There's lots of things you could use. Maybe stay away from NaOH as it eats/etches glass. Why not just pure Niacin powder and sodium carbonate?
|
|
|
Hexavalent
International Hazard
Posts: 1564
Registered: 29-12-2011
Location: Wales, UK
Member Is Offline
Mood: Pericyclic
|
|
Would sodium carbonate even work for this type of decarboxylation?
What we've discussed here is a type that uses copper as a catalyst in some way.
"Success is going from failure to failure without loss of enthusiasm." Winston Churchill
|
|
|
SM2
Hazard to Others
Posts: 359
Registered: 8-5-2012
Location: the Irish Springs
Member Is Offline
Mood: Affect
|
|
| Quote: Originally posted by Hexavalent | Can you please word your answer slightly better? Got what right? Do you mean the thermal decomposition?
What do you mean by 1/3 NaOH (and do you also mean CaO)? Writing formulae correctly really helps other people interpret your suggestions and answers.
According to what I've read, both in the paper and what I was told by Polverone, no additional solids are needed, just to heat the copper complex in a
distillation rig is sufficient. I could perhaps understand why Ca(OH)2 could be added, perhaps to absorb some of the CO2, but that's as far as I can
understand with what you've written so far.
[Edited on 18-5-2012 by Hexavalent] |
so sorry to but in, buy I am fairly certain you got the general gist of what Jon was saying. Perhaps his English is poor. In any event, more
information is better, and should be encouraged, not belittled.
OK, on further review, he needs some serious help. I'll leave it at that!
[Edited on 10-8-2012 by Fennel Ass Ih Tone]
|
|
|
ScienceHideout
Hazard to Others
Posts: 391
Registered: 12-3-2011
Location: In the Source
Member Is Offline
Mood: High Spin
|
|
Now the only question is... where to get niacin ... Can it be extracted from
cigarettes? Even that is sorta difficult now because a pack of cigs in MI are almost $7... wow...
hey, if you are reading this, I can't U2U, but you are always welcome to send me an email!
|
|
|
Lambda-Eyde
National Hazard
Posts: 860
Registered: 20-11-2008
Location: Norway
Member Is Offline
Mood: Cleaved
|
|
Niacin is also known as vitamin B<sub>3</sub> and can be bought as a pure powder in kilogram quantities on eBay. You seriously have to be
clinically insane to make pyridine (in visible amounts) from niacin extracted from cigarettes (if it contains any at all). Insane and insanely rich.
And a lot of spare time and patience.
This just in: 95,5 % of the world population lives outside the USA
Please drop by our IRC channel: #sciencemadness @ irc.efnet.org
|
|
|
Dr.Bob
International Hazard
Posts: 2734
Registered: 26-1-2011
Location: USA - NC
Member Is Offline
Mood: No Mood
|
|
Or you could just buy the bottle of pyridine on Ebay for not much more:
http://www.ebay.com/itm/Karl-fischer-reagent-pyridine-free-5...
|
|
|
runne
Harmless
Posts: 2
Registered: 4-4-2008
Member Is Offline
Mood: No Mood
|
|
*cough* Pyridine free
|
|
|
Mailinmypocket
International Hazard
Posts: 1351
Registered: 12-5-2011
Member Is Offline
Mood: No Mood
|
|
This supplier unfortunately only ships to the USA  He claims international shipping
however to ship anywhere else in the world is ridiculous... he charges $900,000.00 to send the pyridine to Canada.
The lowest shipping cost he charges (for Canada anyways) is $86 and that is to send something like 5g of luminol. I guess he just wants his items to
appear in all eBay searches, unless there is somebody in the USA who can receive the item and re-ship it...which would work but would be a hassle
probably.
|
|
|
Dr.Bob
International Hazard
Posts: 2734
Registered: 26-1-2011
Location: USA - NC
Member Is Offline
Mood: No Mood
|
|
My bad. There used to be people selling it on Ebay as Karl Fisher Reagent. I know several people that have to those annoying titration tests often.
Not sure what they have substituted for it now.
Sorry, false alarm.
Bob
|
|
|
FJS
Harmless
Posts: 4
Registered: 3-4-2013
Member Is Offline
Mood: No Mood
|
|
| Quote: Originally posted by ubungy | I ran the reaction of niacin with CuCO3.Cu(OH)2 in place of the copper chromite catalyst as per the directions in Magpie's thread, and recommendations in this thread. I hope it is okay to share my results here.
Few years ago when I saw that post like anyone when seeing new names like Copper chromite backed off! lol but think the knowledge all comes from
searching and searching or better says googling and googling. now believe making Pyriding could be absolutely OTC consider current web resources.
firstly for making copper chromite, as original post by magpie says ... read on below:
A. Preparation of Copper Chromite
Cu(NO3)2 + Ba(NO3)2 + (NH4)2Cr2O7 ---> complex chromates ---(ignition)---> Cr2CuO4•CuO•BaCrO4 + gases (likely NOx + NH3 + H2O)
if you youtube you can easily find out how to make CU derivations, like sulfate (think by user Nerdrage) or even nitrate etc. then you need Ba
element, the nitrate one. for this one just use sparkle in water as Youtube instructed. for the rest that's is same as before. just type Ammunium
chromate in youtube. now you have all 3 regent for making copper chromite!
Personally I have not done Copper Chromite but gone up to making Copper II sulfate by own and it was easy for someone who not knowing much about
chemistry.
For Niacin I plan to use waste water from Shoshah bang that in Akl is very common in cafe. it's a kind of tabaco that use a kind of device called
Shisha or Shosha not knowing what's that. but believe the waste contain rich Niacin derivations.
Anyway hope that's help but not sure how accurate be my assumptions as explained not tried but theoretically should work or other expert correct or
refine it.
Cheers
|
|
|
|
paw_20
Harmless
Posts: 32
Registered: 14-8-2012
Location: United States
Member Is Offline
Mood: Curious
|
|
Do you mean a hookah? The device that is, a water bong sort of contraption with 1 or more hoses to smoke from. Shisha is the tobacco blend used in
hookahs, very sticky and full of flavorings and such. One trick is to replace the water in the hookah with milk, makes for a very smooth smoke. It was
the one time I tried it anyway.
I wouldn't bet on extracting much nicotine or nicotinic acid from shisha and/or hookah waste, for the same reasons Lambda posted above. Also because a
lot of the nicotine will have already been removed from the shisha by smoking.
|
|
|
| Pages:
1
2 |
![[*]](images/xpblue/default_icon.gif){kind=icon}
