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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815948Generated: October 31, 2026

Benzyl Bromide → 4-(Benzyloxy)-2-fluorobenzonitrile

https://huagongshe.com/reaction/1815948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-4-hydroxybenzonitrileHCID 2734675—
SolventAcetoneHCID 180—
Product4-(Benzyloxy)-2-fluorobenzonitrileHCID 11333628—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2-fluoro-4-hydroxybenzonitrile (15.0 g, 109 mmol), potassium carbonate (21.0 g, 152 mmol), and benzyl bromide (19.6 g, 115 mmol) in acetone (150 mL) under nitrogen was heated at 50° C. overnight. The solid was removed by filtration and the filtrate evaporated to a residue that was mixed with ethyl acetate (500 mL). This solution was washed with brine, dried, and evaporated to give an amorphous solid: (24.9 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881749B2
Source datasetuspto-grants-2005_04
ORD IDord-6dc1315e4eaf4d598b2284bdd80f843f
Source noteuspto-grants-2005_04