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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383742Generated: October 31, 2026

4-Bromobenzyl bromide → 4-broMobenzyl)(Methyl)sulfane

https://huagongshe.com/reaction/383742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzyl bromideHCID 68527—
ReactantSodium methanethiolateHCID 4378561—
SolventTetrahydrofuranHCID 8028—
Product4-broMobenzyl)(Methyl)sulfaneHCID 12587517—

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium thiomethoxide (1.0 g, 14.3 mmol) and 4-bromobenzyl bromide (2.65 g, 10.6 mmol) were combined with anhyd THF (50 mL) and the reaction mixture was stirred at 60° C. After 3 h the reaction mixture was concentrated in vacuo and the residue was washed into a separatory funnel with EtOAc and water. The organic layer was separated, dried (anhyd MgSO4), and concentrated in vacuo to yield 1-bromo-4-methylthiomethyl-benzene. To a solution of this crude thioether in DCM (100 mL) was added 3-chloroperoxybenzoic acid (77%, 4.0 g) portionwise. After stirring overnight the reaction mixture was poured into a separatory funnel, washed with 1N NaOH, dried (Na2SO4), and concentrated in vacuo. The residue was crystallized from EtOAc-Hex to afford 1-bromo-4-methanesulfonylmethyl-benzene (2.02 g, 76%) as light tan needles:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367667B2
Source datasetuspto-grants-2013_02
ORD IDord-6243c3ab7f544a968e186924c7da879e
Source noteuspto-grants-2013_02