Synthesis 2003(15): 2289-2291  
DOI: 10.1055/s-2003-41077
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York

Oxidation of the Methyl Group at the Aromatic Nucleus with Molecular Oxygen­ in the Presence of N-Bromosuccinimide under Photoirradiation

Akichika Itoh*, Tomohiro Kodama, Shouei Hashimoto, Yukio Masaki
Gifu Pharmaceutical University, Mitahora-higashi, Gifu 502-8585, Japan
e-Mail: itoha@gifu-pu.ac.jp;
Further Information

Publication History

Received 25 April 2003
Publication Date:
23 September 2003 (online)

Abstract

A methyl group at the aromatic nucleus can be oxidized to the corresponding carboxylic acid directly in the presence of N-bromosuccinimide (NBS) under photoirradiation. By considering both the promoting effect of oxygen and a catalytic amount of NBS, aerobic oxidation via hydroperoxide, which is thought to be generated by abstraction of a hydrogen with a bromo radical from NBS, proceeded.

6

The corresponding aldehydes (6-7%) and inseparable products were formed, respectively.

7

4-tert-Butylbenzaldehyde was oxidized to 2 in 93% yield under the same reaction conditions.