Issue 16, 2021

1,1,2-Tribromoethyl arenes: novel and highly efficient precursors for the synthesis of 1-bromoalkynes and α-bromoketones

Abstract

In this work, we developed a novel method to synthesize 1,1,2-tribromoethyl arenes, which can be easily transformed to 1-bromoalkynes via base-mediated elimination reaction. The bromination reagent was in situ generated from the reaction of NaBr/NaBrO3/H2SO4, resulting in high reactivity, excellent chemical selectivity and outstanding functional group tolerance. Moreover, 1,1,2-tribromoethyl arenes encounter a selectivity switch to afford α-bromoketones under strong acidic conditions.

Graphical abstract: 1,1,2-Tribromoethyl arenes: novel and highly efficient precursors for the synthesis of 1-bromoalkynes and α-bromoketones

Supplementary files

Article information

Article type
Research Article
Submitted
23 May 2021
Accepted
05 Jul 2021
First published
09 Jul 2021

Org. Chem. Front., 2021,8, 4387-4391

1,1,2-Tribromoethyl arenes: novel and highly efficient precursors for the synthesis of 1-bromoalkynes and α-bromoketones

X. Lin, C. Fang, X. Huang and X. Xiao, Org. Chem. Front., 2021, 8, 4387 DOI: 10.1039/D1QO00793A

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