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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977477Generated: October 30, 2026

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

https://huagongshe.com/reaction/1977477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
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 portioned 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) δ7.62 (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 numberUS06232342B1
Source datasetuspto-grants-2001_05
ORD IDord-4abddbc492ef4ec8a02587317c157512
Source noteuspto-grants-2001_05