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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18422Generated: October 26, 2026

3-Bromobenzyl bromide → 3-Bromobenzylmethylsulfone

https://huagongshe.com/reaction/18422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromobenzyl bromideHCID 69979—
ReactantSodium methanesulfinateHCID 2733271—
SolventDimethylformamideHCID 6228—
Product3-BromobenzylmethylsulfoneHCID 276141667%

Reaction Steps

A solution of 3-bromobenzyl bromide (5.0 g, 20 mmol) in dry dimethylformamide (50 ml) at room temperature under an atmosphere of argon was treated portionwise with sodium methanesulfinate (2.0 g, 20 mmol) with stirring. The mixture was stirred at room temperature for 16 h, and then at 50° C. for 0.5 h. The reaction mix was allowed to cool to room temperature and then partitioned between ethyl acetate and water. The organic layer was separated and dried over sodium sulfate and the solvent removed under reduced pressure to give an oil which was purified by column chromatography on a 50 g isolute silica sep-pak column eluting from 0-100% ethyl acetate in petroleum ether to give the title compound as an off-white solid (3.34 g, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741351B2
Source datasetuspto-grants-2010_06
ORD IDord-46b8d8503a9e4212bad9578f9f61605b
Source noteuspto-grants-2010_06