Switchable Synthesis of Sulfoxides, Sulfones and Thiosulfonates through Selectfluor-Promoted Oxidation with H2O as O-Source
Xuqiang Guo, Sun Xuejun, Yulei Zhao, Mengmeng Jiang
Abstract
Abstract A practical and efficient protocol for the switchable synthesis of sulfoxides, sulfones, and thiosulfonates via Selectfluor-mediated oxidation of sulfides and thiols, respectively, at ambient temperature has been developed. All these organosulfur compounds can be prepared with nearly quantitative yields by applying eco-friendly H2O as O-source. The formation of sulfoxides and thiosulfonates takes only a few minutes (3–20 min). As suggested by the control experiments, the oxidation procedure might proceed through the fluorination of sulfide, nucleophilic addition with H2O, and elimination of hydrogen fluoride.
Topics & Concepts
ChemistrySelectfluorNucleophileOrganosulfur compoundsSulfideHydrogen sulfideCombinatorial chemistrySulfurOrganic chemistryReagentCatalysisSulfur-Based Synthesis TechniquesChemical Synthesis and ReactionsSynthesis and Catalytic Reactions