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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357667Generated: November 1, 2026

p-Tolyl methyl sulfone → 2-Bromo-4-(methanesulfonyl)-1-methylbenzene

https://huagongshe.com/reaction/2357667

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Tolyl methyl sulfoneHCID 18521—
ReactantBromineHCID 24408—
ReactantSodium ThiosulfateHCID 24477—
CatalystIronHCID 23925—
SolventEthyl AcetateHCID 8857—
Product2-Bromo-4-(methanesulfonyl)-1-methylbenzeneHCID 5321698775.1%

Reaction Steps

To a suspension of iron powder (0.0669 g, 1.20 mmol) in bromine (2.05 mL, 39.9 mmol) at 0° C. was added methyl p-tolyl sulfone (0.340 g, 2.00 mmol). The reaction was warmed up to RT and stirred for 2 h. The mixture was poured into an ice-cold 1 M solution of sodium thiosulfate and ethyl acetate. The layers were separated and the aqueous layer was extracted with ethyl acetate (3×). The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated to give 545 mg of crude material. The crude material was purified by column chromatography (3/1 Hex/ethyl acetate to 1/1 ethyl acetate/hexanes) to give 374 mg of 2-bromo-1-methyl-4-(methylsulfonyl)benzene as a white solid. ES+=251.0 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-ccfecc2491fa430cb8ec2a37f7d28238
Source noteuspto-grants-2010_07