Delépine reaction

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) ^{[1] [2]}. It is named after the French chemist Stéphane Marcel Delépine (1871–1965).

Additional recommended knowledge

Don't let static charges disrupt your weighing accuracy

Correct Test Weight Handling Guide: 12 Practical Tips

Recognize and detect the effects of electrostatic charges on your balance

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 ^[3].

Reaction mechanism

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.

References

1. ^ M. Delépine: Bull.Soc.Chim.Fr.. 1895, 13, S. 352 - 361
2. ^ Alexander R. Surrey: Name Reactions in Organic Chemistry. 2nd Edition, Academic Press, 1961
3. ^ 2-bromoallylamine Albert T. Bottini, Vasu Dev, and Jane Klinck Organic Syntheses, Coll. Vol. 5, p.121 (1973); Vol. 43, p.6 (1963).