Electrochemical Synthesis of α,α-Dichlorosulfoxides from Methyl Sulfoxides with Dichloromethane
A novel electrochemical method for chlorination reactions which use methyl sulfoxides and dichloroethane to synthesize derivatives of α,α-dichlorosulfoxides has been developed. The reaction proceeds under mild conditions without transition metals and chemical oxidants in yields of up to 78%. In addition, mechanistic studies reveal that dichloromethane provides the chlorine source under electrolytic conditions. This strategy further expands the synthetic methods for <i>gem</i>-dichlorosulfoxides and provides a new approach to utilize dichloromethane as a chlorine source.
Authors
- Jiacheng Sun (ORCID: https://orcid.org/0009-0008-0133-7867)
- Xuke Liu
- Xiang Liu (ORCID: https://orcid.org/0000-0002-0213-637X)
- Ying Zhao
- Wenjing Yang
- Shu-Yong Song
- Fengshi Sun
Institutions
- Academy of Medical Sciences (GB)
- Shanghai Institute of Materia Medica (CN)
- Shandong First Medical University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-01-14
- DOI
- https://doi.org/10.1021/acs.joc.5c02771
- Primary Topic
- Vanadium and Halogenation Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00