Issue 0, 1968

The Friedel-Crafts acylation of aromatic halogen derivatives. Part III. The benzoylation of chlorobenzene

Abstract

The Friedel-Crafts benzoylation of chlorobenzene leads to mixtures of o-(3–12%), m-(0.1–4%), and p-(84–97%) chlorobenzophenones and benzophenone (0–8%). The effects of solvent, catalyst, mode of addition, temperature, and duration of the reaction have been examined. The reactivity ratio of chlorobenzene: benzene has been found to be 0.0260 in nitrobenzene solution at 25°, leading to the partial rate factors of= 0.00328, mf= 0.00016, and pf= 0.150.

Article information

Article type
Paper

J. Chem. Soc. C, 1968, 966-969

The Friedel-Crafts acylation of aromatic halogen derivatives. Part III. The benzoylation of chlorobenzene

P. A. Goodman and P. H. Gore, J. Chem. Soc. C, 1968, 966 DOI: 10.1039/J39680000966

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