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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394875Generated: October 28, 2026

4-Bromophenacyl bromide → 1-(4-Bromophenyl)-2-fluoroethan-1-one

https://huagongshe.com/reaction/394875

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromophenacyl bromideHCID 7454—
Reactant18-Crown-6HCID 28557—
ReactantPotassium FluorideHCID 522689—
SolventAcetonitrileHCID 6342—
Product1-(4-Bromophenyl)-2-fluoroethan-1-oneHCID 10036278102.1%

Reaction Steps

A mixture of 2-bromo-1-(4-bromophenyl)-1-ethanone (8.54 g, 30.7 mmol), potassium fluoride (8.92 g, 153 mmol) and 18-crown-6 ether (4.06 g, 15.3 mmol) in acetonitrile (170 ml) was refluxed for 7 hr. After evaporation, the mixture was dissolved in ethyl acetate (300 ml), washed with water (100 ml×2), and dried over magnesium sulfate. Removal of solvent gave 6.8 g of brown solid, which was chromatographed on a column of silica gel (600 g) eluting with ethyl acetate/hexane (1:10) to afford 5.00 g (75%) of the title compound as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06603008B1
Source datasetuspto-grants-2003_08
ORD IDord-e383e9eb5ec74fb6bdf7e514782f51bb
Source noteuspto-grants-2003_08