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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389361Generated: November 1, 2026

Benzyl Bromide → 2-(3-(Benzyloxy)phenyl)ethanol

https://huagongshe.com/reaction/2389361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Hydroxyphenethyl alcoholHCID 83404—
SolventAcetoneHCID 180—
Product2-(3-(Benzyloxy)phenyl)ethanolHCID 20402544—

Reaction Steps

To a solution of 3-(2-hydroxyethyl)phenol (1.0 g) and K2CO3 (1.5 g) in acetone (20 mL) was added (bromomethyl)benzene (1.49 g) at ambient temperature. The reaction mixture was stirred at the same temperature for 17 hours. The resulting mixture was evaporated in vacuo. The residue was diluted with EtOAc and washed successively with water and brine. The organic layer was dried over anhydrous MgSO4, filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography (n-hexane:EtOAc=90:10-70:30) to give 2-[3-(benzyloxy)phenyl]ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273745B2
Source datasetuspto-grants-2012_09
ORD IDord-3d76e9a5a6e24fa49c6a95691779074c
Source noteuspto-grants-2012_09