SO₂F₂-mediated transformation of 2'-hydroxyacetophenones to benzo-oxetes

Abstract

A catalyst-free novel and efficient methodology for the challenging synthesis of benzo-oxetes from 2'-hydroxyacetophenones mediated by sulfuryl fluoride (SO 2 F 2 ) gas has been realized. The combination of 2'-hydroxyacetophenones and SO 2 F 2 furnishes synthetically challenging benzo-oxetanes in moderate to excellent yields. The highlight of this work is the design and synthesis of strained four-membered oxete rings.