Issue 8, 1970

Bromination of copper chelates of monoarylhydrazones of triketones

Abstract

3-Arylhydrazones of pentane-2,3,4-triones are known to undergo substitutive bromination. We report here a study of the bromination of the copper chelates of arylhydrazones of pentane-2,3,4-trione and 5,5-dimethylcyclohexane-1,2,3-trione. The products, 3-arylazo-3-bromopentane-2,4-diones and 2-arylazo-2-bromo-5,5-dimethylcyclohexane-1,3-diones, liberate iodine from acidified potassium iodide solution.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 1056-1057

Bromination of copper chelates of monoarylhydrazones of triketones

H. C. Garg and C. Prakash, J. Chem. Soc. C, 1970, 1056 DOI: 10.1039/J39700001056

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