Issue 0, 1968

Studies on benzimidazoles. Part IV. Nucleophilic displacement of N-substituted 2-halogenobenzimidazoles by thiophenol

Abstract

2-Halogenobenzimidazoles react with thiophenol as well as with benzenethiolate ion. The reaction also occurs in acidic medium. The effect on the reaction of structural modifications in the benzimidazole and in the thiophenol have been investigated. The general kinetic equation Rate =k1[B][ArS]+k2[BH+][ArSH]+k3[BH+][ArS] is proposed to explain the overall reaction.

Article information

Article type
Paper

J. Chem. Soc. B, 1968, 1280-1284

Studies on benzimidazoles. Part IV. Nucleophilic displacement of N-substituted 2-halogenobenzimidazoles by thiophenol

A. Ricci and P. Vivarelli, J. Chem. Soc. B, 1968, 1280 DOI: 10.1039/J29680001280

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