Issue 16, 1978

Novel synthesis of benzotrihalides: the pyrolysis of phenyl trihalogenoacetates

Abstract

Pyrolysis of 4-chlorophenyl trichloroacetate (I) at 500 °C yields 4-chlorobenzotrichloride (II) and some 1,4-dichlorobenzene (III) as by-product; the corresponding trifluoroacetate is converted into 4-chlorobenzotrifluoride.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 714a-714a

Novel synthesis of benzotrihalides: the pyrolysis of phenyl trihalogenoacetates

R. G. Pews and R. A. Davis, J. Chem. Soc., Chem. Commun., 1978, 714a DOI: 10.1039/C3978000714A

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