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Synthesis 2003(15): 2289-2291
DOI: 10.1055/s-2003-41077
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
Further Information
Received
25 April 2003
Publication Date:
23 September 2003 (online)
Publication History
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.
Key words
oxidations - methyl group - N-bromosuccinimide - photoirradiation - molecular oxygen
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References
The corresponding aldehydes (6-7%) and inseparable products were formed, respectively.
74-tert-Butylbenzaldehyde was oxidized to 2 in 93% yield under the same reaction conditions.