Issue 19, 2024

Photoelectrochemical synthesis of 4-halomethyl benzoxazines with a halogen anion source

Abstract

Benzoxazine is an important motif in various pharmaceuticals and functional molecules. We herein described a visible-light induced photoelectrochemical strategy for the synthesis of 4-halomethyl benzoxazines with an organo-photocatalyst. In the present protocol, a series of olefinic amides can be transformed into 4-halomethyl benzoxazines via oxyhalogenation with nBu4NX as the halogenating reagent, showing good functional group tolerance.

Graphical abstract: Photoelectrochemical synthesis of 4-halomethyl benzoxazines with a halogen anion source

Supplementary files

Article information

Article type
Research Article
Submitted
12 Jun 2024
Accepted
12 Aug 2024
First published
14 Aug 2024

Org. Chem. Front., 2024,11, 5553-5557

Photoelectrochemical synthesis of 4-halomethyl benzoxazines with a halogen anion source

X. Chen, X. Li, H. Dai, Y. Wang, Z. Wu and W. He, Org. Chem. Front., 2024, 11, 5553 DOI: 10.1039/D4QO01068J

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