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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594977Generated: October 30, 2026

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

https://huagongshe.com/reaction/1594977

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
Product1-(Benzyloxy)-2-bromobenzeneHCID 561828100%

Reaction Steps

To a stirring solution of 2-bromophenol (10.0 g, 57.8 mmol), and benzyl bromide (9.9 g, 57.8 mmol) in acetone (150 mL) was added K2CO3 (12.0 g, 86.7 mmol). After stirring at reflux for 4h, the mixture was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried (MgSO4), filtered and concentrated. The residue was purified by column chromatography (silica gel, ethyl acetate/hexane) to yield the title compound as a colorless oil (15.2 g, 57.8 mmol), 1HNMR (400 MHz, CDCl3) δ 7.62 (m, 1H), 7.54 (m, 2H), 7.45 (m, 2H), 7.37 (m, 1H), 7.28 (m, 1H), 6.98 (m, 1H), 6.91 (m, 1H), 5.17 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284777B1
Source datasetuspto-grants-2001_09
ORD IDord-c2b4f5bb9c3c4c9883cd23c6953f603b
Source noteuspto-grants-2001_09