Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254134Generated: October 30, 2026

Benzyl Bromide → 1-Bromo-4-phenylmethoxybenzene

https://huagongshe.com/reaction/254134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant4-BromophenolHCID 7808—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product1-Bromo-4-phenylmethoxybenzeneHCID 138835—

Reaction Steps

4-Bromophenol (2 g, 0.0116 mol) in acetone (40 mL) was treated with potassium carbonate anhydrous (1.91 g, 1.2 equivalents) and benzyl bromide (1.44 mL, 1.05 equivalents). The reaction was refluxed under a nitrogen atmosphere. After 5-6 hours reflux, the reaction was cooled to room temperature and diluted with an equal volume of ethyl acetate. This solution was washed with water, dried over anhydrous magnesium sulfate and evaporated to dryness. A white fluffy solid was obtained. Yield=2.36 g (73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875467B2
Source datasetuspto-grants-2011_01
ORD IDord-a1cd9b1875ed4b24b8af85eae921206d
Source noteuspto-grants-2011_01