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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420839Generated: October 29, 2026

Dichloromethane → 2-Bromophenylmethylsulfoxide

https://huagongshe.com/reaction/1420839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2-BromothioanisoleHCID 88166—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-BromophenylmethylsulfoxideHCID 11074873113.2%

Reaction Steps

Oxone (9.7 g) in water (40 ml) was added slowly to a stirred, cooled cooled (0° C.) solution of 2-bromothioanisole (5 g, 24.6 mmol) and sodium bicarbonate (16 g) in acetone (20 ml). The mixture was stirred for at room temperature 16 h., then water and dichloromethane was added. The layers were separated and the organic phase was dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by chromatography on silica gel, eluting with hexane/EtOAc (80:20 increasing to 40:60) to give the title compound (6.1 g). m/z (ES+) 219 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071927
Source datasetuspto-grants-2000_06
ORD IDord-05da3fab12bc48b6b6030ec94b6d3426
Source noteuspto-grants-2000_06