Issue 0, 1968

The reactions of o-nitrobenzaldehydes with bases

Abstract

The reactions of some o-nitrobenzaldehydes with hydroxide and methoxide ions have been studied. Both reagents effect cleavage of the aldehyde to a substituted benzene and either formic acid or methyl formate. Kinetic studies indicate that the cleavage involves a hemi-acetal ion as an intermediate.

Article information

Article type
Paper

J. Chem. Soc. B, 1968, 205-207

The reactions of o-nitrobenzaldehydes with bases

E. J. Forbes and M. J. Gregory, J. Chem. Soc. B, 1968, 205 DOI: 10.1039/J29680000205

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