Convenient ring-bromination of alkylnaphthalenes using N-bromosuccinimide in acetonitrile

Cammidge, Andrew N., Crepy, Karen V. and Fugier, Matthieu (1997) Convenient ring-bromination of alkylnaphthalenes using N-bromosuccinimide in acetonitrile. Synthetic Communications, 27 (23). pp. 4159-4162. ISSN 0039-7911

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Abstract

1-Alkyl- and 2-alkylnaphthalenes are conveniently brominated in the 4-and 1-positions respectively using N-bromosuccinimide (NBS) in acetonitrile. The reactions are easy to perform and give higher chemical yields and better regioselectivity compared to brominations employing bromine/dichloromethane.

Item Type:	Article
Faculty \ School:	Faculty of Science > School of Chemistry (former - to 2024)
UEA Research Groups:	Faculty of Science > Research Groups > Chemistry of Materials and Catalysis Faculty of Science > Research Groups > Synthetic Chemistry (former - to 2017) Faculty of Science > Research Groups > Chemistry of Light and Energy
Depositing User:	Rachel Smith
Date Deposited:	24 Nov 2010 14:50
Last Modified:	28 Mar 2025 05:02
URI:	https://ueaeprints.uea.ac.uk/id/eprint/11005
DOI:	10.1080/00397919708005463

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