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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015738Generated: November 2, 2026

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

https://huagongshe.com/reaction/1015738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Fluoro-3-(methylsulfonyl)benzenemethanolHCID 66877838—
SolventAcetonitrileHCID 6342—
Product4-(Bromomethyl)-1-fluoro-2-(methylsulfonyl)benzeneHCID 66877626—

Reaction Conditions

Temperature85 °C

Reaction Steps

(Step 1) Triphenylphosphine (3.21 g) was suspended in acetonitrile (50 ml), bromine (0.64 ml) was added, and the mixture was stirred for 30 min. [4-Fluoro-3-(methylsulfonyl)phenyl]methanol (2.5 g) was added to the reaction mixture, and the mixture was stirred at 85° C. for 20 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-fluoro-2-(methylsulfonyl)benzene (1.64 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985862B2
Source datasetuspto-grants-2011_07
ORD IDord-e22669d33ceb455d86bf8ed2144fa0c8
Source noteuspto-grants-2011_07