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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672667Generated: October 26, 2026

Salicyl Alcohol → [2-(2-Chlorobenzyloxy)phenyl]methanol

https://huagongshe.com/reaction/1672667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicyl AlcoholHCID 5146—
ReactantPotassium CarbonateHCID 11430—
Reactantalpha-Bromo-o-chlorotolueneHCID 11905—
SolventAcetonitrileHCID 6342—
Product[2-(2-Chlorobenzyloxy)phenyl]methanolHCID 96159279.6%

Reaction Steps

A solution of 2.42 g (19.47 mmol) of 2-hydroxybenzyl alcohol in 100 ml of dry acetonitrile is mixed with 4.12 g (19.47 mmol) of 2-chlorobenzyl bromide and 2.96 g (21.42 mmol) of anhydrous potassium carbonate and heated to reflux for 12 hours. The mixture is then concentrated to dryness. The residue is taken up in ethyl acetate, washed with water and saturated sodium chloride solution and dried over sodium sulfate. The organic phase is concentrated. The resulting crude product is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 7:3). 3.856 g (15.5 mmol, 79% yield) of a solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998988B2
Source datasetuspto-grants-2011_08
ORD IDord-8e3f0e4268514c848443ca63c3a9b4c0
Source noteuspto-grants-2011_08