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

Andrew N. Cammidge; Karen V. Crepy; Matthieu Fugier

doi:10.1080/00397919708005463

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

Andrew N. Cammidge, Karen V. Crepy, Matthieu Fugier

Research output: Contribution to journal › Article › peer-review

15 Citations (Scopus)

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.

Original language	English
Pages (from-to)	4159-4162
Number of pages	4
Journal	Synthetic Communications
Volume	27
Issue number	23
DOIs	https://doi.org/10.1080/00397919708005463
Publication status	Published - 23 Dec 1997

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10.1080/00397919708005463

Cite this

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title = "Convenient ring-bromination of alkylnaphthalenes using N-bromosuccinimide in acetonitrile",

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.",

author = "Cammidge, {Andrew N.} and Crepy, {Karen V.} and Matthieu Fugier",

year = "1997",

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T1 - Convenient ring-bromination of alkylnaphthalenes using N-bromosuccinimide in acetonitrile

AU - Cammidge, Andrew N.

AU - Crepy, Karen V.

AU - Fugier, Matthieu

PY - 1997/12/23

Y1 - 1997/12/23

N2 - 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.

AB - 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.

U2 - 10.1080/00397919708005463

DO - 10.1080/00397919708005463

M3 - Article

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JO - Synthetic Communications

JF - Synthetic Communications

IS - 23

ER -