Electrophilic (Ethoxycarbonyl)difluoromethylthiolation Using Difluoroalkyl Sulfonium Salts

Author:

Liang Weijian1,Li Kaixiao2,Zhang Yage1,Zhou Lijiang1

Affiliation:

1. College of Chemistry and Life Sciences, Zhejiang Normal University

2. College of Physical Education and Health Sciences, Zhejiang Normal University

Abstract

AbstractWe report a simple protocol for (ethoxycarbonyl)difluoromethylthiolation of nucleophilic compounds using a difluoroalkyl sulfonium salt which can be prepared in situ via Tf2O-triggered electrophilic activation of a benzyl difluoroalkyl sulfoxide. With the protocol, difluoroalkylthiolated arenes, heteroarenes, α-difluoroalkylthiolated carbonyl compounds, etc. were obtained smoothly with good to excellent yields. Merits of the reaction include the readily available difluoroalkylthiolation reagent and substrates, mild conditions, and excellent regioselectivity.

Funder

Zhejiang Normal University

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

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