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The Delépine reaction is the organic synthesis of primary amines (4) by acid hydrolysis of a quaternary hexamethylenetetramine salt (3), obtained from alkylation of hexamethylenetetramine (2) with benzyl or alkyl halides (1)  . It is named after the French chemist Stéphane Marcel Delépine (1871–1965).
Additional recommended knowledge
Advantages of this reaction are selective access to the primary amine without side reactions from easily accessible reactants with short reaction times and relatively mild reaction conditions.
An example is the synthesis of 2-bromoallylamine from 2,3-dibromopropene .
The benzyl halide or alkyl halide 1 reacts with hexamethylenetetramine to a quaternary ammonium salt 3, each time just alkylating one nitrogen atom. By refluxing in concentrated ethanolic hydrochloric acid solution this salt is converted to the primary amine together with formaldehyde (as the acetal with ethanol) and ammonium chloride.
|This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Delépine_reaction". A list of authors is available in Wikipedia.|