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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610111Generated: November 1, 2026

Water → (5-Bromo-2-fluoro-4-methoxy-phenyl)-(3-fluoro-phenyl)-methanone

https://huagongshe.com/reaction/1610111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Fluorobenzoyl chlorideHCID 74376—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Bromo-5-fluoroanisoleHCID 7018043—
SolventDichloromethaneHCID 6344—
Product(5-Bromo-2-fluoro-4-methoxy-phenyl)-(3-fluoro-phenyl)-methanoneHCID 22260993—

Reaction Conditions

Temperature-60 °C

Reaction Steps

A total of 716 mg of aluminium chloride was suspended in 24.4 ml of dichloromethane and was then mixed with 0.65 ml of 3-fluorobenzoyl chloride and 1 g of 1-bromo-4-fluoro-2-methoxy-benzene obtained in Production Example II-1-a under stirring at −60° C. The mixture was raised in temperature to room temperature over 2.5 hours and was stirred for further 3 hours. Water was added to the reaction mixture under ice-cooling, followed by extracting with diethyl ether. The resulting organic layer was washed with saturated aqueous sodium hydrogencarbonate solution and brine, dried over magnesium sulfate and the solvent was evaporated. The residue was purified and separated by silica gel column chromatography (ethyl acetate:hexane=1:10), to give 856 mg of the title compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982274B2
Source datasetuspto-grants-2006_01
ORD IDord-43f23cd3818549a7a4f0d104a23ea711
Source noteuspto-grants-2006_01