Issue 8, 1988

The chemistry of benzotriazole. Part 8. A novel two-step procedure for the N-alkylation of amides

Abstract

Benzotriazole, aldehydes RCHO, and amides R1CONH2 react together with elimination of water to form 1:1:1 adducts which are reduced smoothly by NaBH4 to give the N-substituted amides R1CONHCH2R. Both steps occur in high yields and can be carried out on a large scale, thus comprising a convenient general method for the N-alkylation of amides.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1988, 2339-2344

The chemistry of benzotriazole. Part 8. A novel two-step procedure for the N-alkylation of amides

A. R. Katritzky and M. Drewniak, J. Chem. Soc., Perkin Trans. 1, 1988, 2339 DOI: 10.1039/P19880002339

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements