Issue 0, 1987

Carbonylation of aryl halides and vinyl bromides mediated by tetracarbonylcobalt anion

Abstract

The reaction of aryl halides (1ag) with octacarbonyldicobalt in the presence of methyl iodide and sodium hydroxide under phase-transfer conditions was found to give a mixture of aryl methyl ketones (2ag) and aromatic carboxylic acids (3ah). From vinyl halides (9ac), however, the corresponding carboxylic acids (10ac) were obtained exclusively.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1987, 1021-1025

Carbonylation of aryl halides and vinyl bromides mediated by tetracarbonylcobalt anion

M. Miura, F. Akase, M. Shinohara and M. Nomura, J. Chem. Soc., Perkin Trans. 1, 1987, 1021 DOI: 10.1039/P19870001021

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