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N-Methyl Pyrrolidone decomposition Question
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Guest

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Fri May 20, 2005 9:03 pm
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N-Methyl Pyrrolidone

My question is, is it possible to remove the double bond, and then have the option to demethylate?

Suggestions?



Syn
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IndoleAmine
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Joined: 09 Feb 2005
Posts: 681
Location: Bahamas
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Wed May 25, 2005 5:22 pm
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To make pyrrolidine, pyrroline or pyrrole - right? (no, one or two cyclic double bounds?)

What would you want with those five-membered heterocycles? Detroy them to make n-butylamine maybe? Very Happy

As far as about your question, no you can't remove the double bond from a C=O, only add a H to it to make C-OH, reductively. Or even further to the CH alkane by adding more H and splitting off H2O...

(what was/is the goal with such enterprises?)
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Guest

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Sun May 29, 2005 9:45 am
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Thanks indole,

Just a basic chemistry question, as I saw it lying around in a hardware store,
Just looked very close to piperidine, which really has not got any use except if you wanted to remove the H, by boiling in H2SO4 at 300c
It's fascinating stuff, cheers

syn
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Dr.Bunsen

Joined: 20 Feb 2005
Posts: 14
280.86 Points

Sun May 29, 2005 5:59 pm
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I've just found these references:

pyrrolidine from pyrrolidone with sodium

J.Schlinck, B.32, 952 (1899)
L.Ruzicka, Helv. 16, 1323 (1933)


synthetika wrote:



N-Methyl Pyrrolidone

My question is, is it possible to remove the double bond, and then have the option to demethylate?

Suggestions?



Syn
Back to top
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