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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013983Generated: October 30, 2026

Triphenylphosphine → 4-(Bromomethyl)-1-chloro-2-(methylsulfonyl)benzene

https://huagongshe.com/reaction/1013983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-3-(methylsulfonyl)benzenemethanolHCID 53757506—
SolventAcetonitrileHCID 6342—
Product4-(Bromomethyl)-1-chloro-2-(methylsulfonyl)benzeneHCID 66877460—

Reaction Conditions

Temperature85 °C

Reaction Steps

(Step 1) Triphenylphosphine (2.38 g) was suspended in acetonitrile (30 ml), bromine (0.47 ml) was added, and the mixture was stirred for 30 min. [4-Chloro-3-(methylsulfonyl)phenyl]methanol (2.0 g) was added to the reaction mixture, and the mixture was stirred at 85° C. for 8 hr, treated with aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by basic silica gel chromatography (ethyl acetate:hexane=1:1) to give 4-(bromomethyl)-1-chloro-2-(methylsulfonyl)benzene (1.23 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982044B2
Source datasetuspto-grants-2011_07
ORD IDord-9dd6cea4eafe4e139c3ff9c2802cdcec
Source noteuspto-grants-2011_07