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Topic: Pyridine  (Read 9247 times)

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Offline limpet chicken

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Pyridine
« on: December 28, 2004, 04:05:18 PM »
Hello people.

I am having great difficulty finding anything related to the synthesis of pyridine, there are lots of articles relating to synthesis of substituted pyridine, but none I can find for pyridine itself, could someone point me on the way to a synthesis?

The closest I have managed to find, is a possible preperation, as detailed on sciencemadness.org, regarding possible synthesis via reaction of aqueous HCN and acetylene, and further research online showed a few references to reaction of ammonia and nitriles, assisted by a cobalt  or possibly nickel catalyst.

Has anyone had any experience with this synthesis? more in particular the one using HCN/acetylene, could this perhaps be done in the gas phase even? and the pyridine condensed out via continuous distillation into HCl to form the hydrochloride salt, this synthesis would be a geat deal more practical for me than the nitrile one due to availability of reactants.

What about passing heated HCN and acetylene through a tube over cobalt metal plated on carbon, or the chloride salt on rockwool, then condensing the product (hopefully) into HCl?

Just an afterthought, there was a thread on pyridine synthesis posted over at the Hive, in serious chemistry discussion, before the server went down, does anyone happen to have that thread saved, or perchance know of a Bee that does?

Thanks people.

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Offline AWK

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Offline limpet chicken

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Re:Pyridine
« Reply #2 on: December 29, 2004, 01:42:16 PM »
Thanks AWK, scooby snack sent your way :)
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Corvettaholic

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Re:Pyridine
« Reply #3 on: December 29, 2004, 06:16:16 PM »
Just out of curiousity... whats pyridine used for?

Offline limpet chicken

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Re:Pyridine
« Reply #4 on: December 29, 2004, 06:30:03 PM »
Pyridine is a nitrogenous base, it can act as a solvent for alkali metal electrolysis, or in the process of demethylating codeine to morphine, just two reactions I can remember offhand, and numerous other organic reaction, also used sometimes as a denaturant for ethanol, as only trace amounts are needed, as it well and truly REEKS of rotting fish.

Pyridine is quite unpleasant though, aside from the stench, it can well and truly do a number on your reproductive system, at least so I have heard.
« Last Edit: December 29, 2004, 06:32:30 PM by limpet chicken »
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Offline Donaldson Tan

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Re:Pyridine
« Reply #5 on: January 02, 2005, 11:08:01 PM »
it's one of the nitrogenous base in the DNA
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Offline limpet chicken

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Re:Pyridine
« Reply #6 on: January 03, 2005, 06:46:34 AM »
Geodome, the bases in DNA are pyrimidines, not pyridines, the four DNA base pairs are the purines adenine and guanine, and the corresponding pyrimidines, thymine and cytosine.
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Offline Donaldson Tan

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Re:Pyridine
« Reply #7 on: January 03, 2005, 08:26:04 PM »
ooo.. spelling.. LOL..
"Say you're in a [chemical] plant and there's a snake on the floor. What are you going to do? Call a consultant? Get a meeting together to talk about which color is the snake? Employees should do one thing: walk over there and you step on the friggin� snake." - Jean-Pierre Garnier, CEO of Glaxosmithkline, June 2006

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