The Journal of Organic Chemistry · 2019 · 42 citations · 43 references
Natural SciencesChemical EngineeringChemistryCatalysisGreen ChemistrySolid-state ChemistryCatalyst DesignCatalyst SynthesisCatalytic MechanismsCrystal ChemistryHeterocycle SynthesisSolvent-free SynthesisCatalytic Reaction MechanismsMulticomponent Reaction ChemistrySolvent-free CatalysisSolvent-free Heterocycle SynthesisSolvent-free ProcessingThiol ChemistryThiosulfate Chemistry
It is observed the crystal water in sodium thiosulfate pentahydrate (Na2S2O3·5H2O) can promote its multicomponent reaction with heteroaryl chlorides and alcohols, providing a facile, green, and specific synthesis of unsymmetrical heteroaryl thioethers via one-step formation of two C–S bonds under catalyst-, additive-, and solvent-free conditions. Mechanistic studies suggest that the crystal water in Na2S2O3·5H2O is crucial in generating the key thiol intermediates and byproduct NaHSO4, which then catalyzes the dehydrative substitution of alcohols with thiols to afford thioethers.
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