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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897480Generated: October 30, 2026

4-Bromophenol → 4-(4-Bromophenoxy)benzonitrile

https://huagongshe.com/reaction/897480

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenolHCID 7808—
Reactant4-FluorobenzonitrileHCID 14517—
Reactant18-Crown-6HCID 28557—
ReactantPotassium FluorideHCID 522689—
SolventAcetonitrileHCID 6342—
Product4-(4-Bromophenoxy)benzonitrileHCID 2234739651.1%

Reaction Steps

A mixture of 4-bromophenol (4.56 g, 0.0264 mol), 4-fluorobenzonitrile (0.0264 mol), 18-Crown-6 (0.7 g, 0.00264 mol) and 40% potassium fluoride on alumina (10.8 g) in anhydrous acetonitrile (100 mL) was heated at reflux under an atmosphere of nitrogen for twelve hours. It was cooled to ambient temperature, filtered through a Celite pad and concentrated under reduced pressure. The residue was partitioned between diethyl ether (120 mL) and water (100 mL), the organic phase was further washed with saturated solution of potassium chloride in water, dried with magnesium sulfate and concentrated. The residue was purified by flash chromatography on silica using ethyl acetate/n-heptane (3:97) as mobile phase to yield 4-(4-bromophenoxy)benzonitrile (3.7 g, 0.0135 mol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921763B2
Source datasetuspto-grants-2005_07
ORD IDord-a42346b2d73849c5b94eed409e61051e
Source noteuspto-grants-2005_07