Enamine

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The general structure of an enamine

An enamine is an unsaturated compound derived by the reaction of an aldehyde or ketone with a secondary amine followed by loss of H₂O.

If one of the nitrogen substituents is H, it is the tautomeric form of an imine. This usually will rearrange to the imine; however there are several exceptions (such as aniline).

[edit] Form

R₂C = CR − NR₂

An analogy may be made between an enol and an ketone or aldehyde and the enamine and an imine.

[edit] See also

• Thorpe reaction

Retrieved from "http://en.wikipedia.org../../../e/n/a/Enamine.html"

Category: Functional groups

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• This page was last modified 02:42, 2 March 2007 by Wikipedia user Betacommand. Based on work by Wikipedia user(s) Olin, ~K, Benjah-bmm27, Eskimbot, YurikBot, DA3N, V8rik, Jgassens, Securiger and Bensaccount and Anonymous user(s) of Wikipedia.
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