Issue 0, 1970

The kinetics and mechanism of electrophilic substitution of heteroaromatic compounds. Part XXI. Bromination of 2-aminopyridines

Abstract

The bromination kinetics for a series of 5-substituted 2-amino- and 2-dimethylamino-pyridines and for some para-substituted anilines are described. The heterocyclic compounds react as their free bases. Results are correlated by the Hammett equation, and the quantitative effect of the aza group in slowing down the rate is discussed.

Article information

Article type
Paper

J. Chem. Soc. B, 1970, 117-121

The kinetics and mechanism of electrophilic substitution of heteroaromatic compounds. Part XXI. Bromination of 2-aminopyridines

P. J. Brignell, P. E. Jones and A. R. Katritzky, J. Chem. Soc. B, 1970, 117 DOI: 10.1039/J29700000117

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