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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983525Generated: October 31, 2026

2-Bromophenol → 1-(Benzyloxy)-2-bromobenzene

https://huagongshe.com/reaction/983525

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
Product1-(Benzyloxy)-2-bromobenzeneHCID 56182894.5%

Reaction Steps

A mixture of 35 g of 1-bromo-2-hydroxybenzene, 30.5 g of benzyl chloride and 50 g of K2CO3 in 500 ml of acetone is refluxed for 12 hours. The reaction mixture is concentrated under vacuum, the residue is taken up in a water/EtOAc mixture, the organic phase is washed with 1N NaOH solution and with water and dried over Na2SO4, and the solvent is evaporated off under vacuum. The resulting oil is distilled under reduced pressure to give 50.3 g of the expected product, b.p.=155° C. at 40 Pa.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864277B2
Source datasetuspto-grants-2005_03
ORD IDord-b8ade4e6503a427ab6350491b97258f8
Source noteuspto-grants-2005_03