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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412106Generated: October 30, 2026

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

https://huagongshe.com/reaction/412106

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 4 h, 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 numberUS06562842B2
Source datasetuspto-grants-2003_05
ORD IDord-142f2204d27a4b90969a435171380e78
Source noteuspto-grants-2003_05