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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610426Generated: November 1, 2026

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

https://huagongshe.com/reaction/610426

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 numberUS05998470
Source datasetuspto-grants-1999_12
ORD IDord-2f1c1a81660c4788a4d471c715865c00
Source noteuspto-grants-1999_12