Divergent Hydroxysulfenylation and Chlorosulfonylation of Styrenes with Sulfinyl Chlorides Steered by Controlled Disproportionation of Sulfoxide‐Onium Ions

Author:

Liang Qingjin1,Jia Tiezheng12ORCID

Affiliation:

1. Research Center for Chemical Biology and Omics Analysis Department of Chemistry Southern University of Science and Technology 1088 Xueyuan Blvd. Shenzhen Guangdong 518055 People's Republic of China

2. State Key Laboratory of Elemento-Organic Chemistry Nankai University Tianjin 300071 People's Republic of China

Abstract

AbstractHerein, sulfinyl chlorides and styrenes have been exploited to afford either β‐hydroxy‐phenylethyl sulfides catalyzed by homogenous ZnCl2, or β‐chloro‐phenylethyl sulfones mediated by heterogeneous CuO nanoparticles (NPs). The key to achieve such a divergent synthetic strategy is the controlled disproportionation process of sulfoxide‐onium ions, induced by different metal complexes. Owing to the mild conditions, a wide range of functional groups and heterocycles could be tolerated by both of the protocols. The mechanistic studies reveal the key role of sulfoxide‐onium ions in both of the reaction pathways, and suggest that metal‐steered disproportionation defines the oxidation state of sulfur in products.

Funder

Basic and Applied Basic Research Foundation of Guangdong Province

Publisher

Wiley

Subject

General Chemistry

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