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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650939Generated: October 29, 2026

Benzyl phenyl sulphide → Benzyl phenyl sulfoxide

https://huagongshe.com/reaction/650939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl phenyl sulphideHCID 13255—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
ProductBenzyl phenyl sulfoxideHCID 239581110.7%

Reaction Steps

To a solution of benzyl phenyl sulfide (Aldrich; 1.068 g, 5.33 mmol) in 25 mL of CH2Cl2 at −78° C. was slowly added a solution of m-chloroperbenzoic acid (Aldrich, 50-60%; 760 mg, 2.64 mmol if 60%) in 10 mL of CH2CL2. After warming to room temperature and stirring overnight, the solution was added to 20 mL of a saturated NaHCO3 solution. The aqueous layer was separated and extracted with CH2Cl2 (2×10 mL). The pooled organic layers were then dried (MgSO4) and concentrated. The residue was subjected to flash column chromatography (silica gel, 10% acetone/hexane and 15% acetone/hexane) affording the sulfoxide (632 mg, 55%) as a white solid, mp 123-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277838B1
Source datasetuspto-grants-2001_08
ORD IDord-aa269e45cf0a4dc79824a237ba086798
Source noteuspto-grants-2001_08