Issue 40, 2023

Visible-light-induced halocyclization of 2-alkynylthioanisoles with simple alkyl halides towards 3-halobenzo[b]thiophenes without an external photocatalyst

Abstract

A new strategy for the preparation of 3-halobenzo[b]thiophenes via a photo-driven halocyclization/demethylation of 2-alkynylthioanisoles with simple alkyl halides was developed. The reaction can proceed smoothly at room temperature under visible-light irradiation without any external photocatalyst, and the protocol has a range of advantages, including simplicity and mildness of the reaction conditions, good functional-group tolerance, and excellent yields of the products.

Graphical abstract: Visible-light-induced halocyclization of 2-alkynylthioanisoles with simple alkyl halides towards 3-halobenzo[b]thiophenes without an external photocatalyst

Supplementary files

Article information

Article type
Paper
Submitted
31 May 2023
Accepted
25 Sep 2023
First published
28 Sep 2023

Org. Biomol. Chem., 2023,21, 8170-8175

Visible-light-induced halocyclization of 2-alkynylthioanisoles with simple alkyl halides towards 3-halobenzo[b]thiophenes without an external photocatalyst

F. Wang, C. Wang, M. Wang, H. Yan, J. Jiang and P. Li, Org. Biomol. Chem., 2023, 21, 8170 DOI: 10.1039/D3OB00860F

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