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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447834Generated: October 30, 2026

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

https://huagongshe.com/reaction/447834

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). 1H NMR (300 MHz, CDCl3) 8 ppm 3.24 (3H, s), 4.49 (2H, s), 7.19-7.31 (1H, m), 7.62-7.74 (1H, m), 7.99 (1H, dd, J=6.50, 2.35 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481569B2
Source datasetuspto-grants-2013_07
ORD IDord-9d8465140fa548818ea2faaeb4f0fb2d
Source noteuspto-grants-2013_07