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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672625Generated: October 27, 2026

Salicyl Alcohol → [2-(4'-Trifluoromethylbiphenyl-4-ylmethoxy)phenyl]methanol

https://huagongshe.com/reaction/1672625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicyl AlcoholHCID 5146—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Trifluoromethylphenyl)benzylchlorideHCID 11459921—
SolventAcetonitrileHCID 6342—
Product[2-(4'-Trifluoromethylbiphenyl-4-ylmethoxy)phenyl]methanolHCID 5786437089.1%

Reaction Steps

A solution of 4.59 g (36.94 mmol) of 2-hydroxybenzyl alcohol in 200 ml of dry acetonitrile is mixed with 10 g (36.94 mmol) of 4-chloromethyl-4′-trifluoromethylbiphenyl from Example 23A and 6.13 g (44.33 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 resulting organic phase is concentrated. The crude product is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 5:1). 11.8 g (32.92 mmol, 89% yield) of a solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998988B2
Source datasetuspto-grants-2011_08
ORD IDord-f156c46a1d504beeb504970a7234d69a
Source noteuspto-grants-2011_08