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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755112Generated: November 2, 2026

Benzyl Alcohol → 3-(Benzyloxy)-4-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1755112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHydrochloric AcidHCID 313—
Reactant3-Fluoro-4-(trifluoromethyl)benzoic acidHCID 688293—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Product3-(Benzyloxy)-4-(trifluoromethyl)benzoic acidHCID 16747844—

Reaction Steps

Potassium tert-butoxide (816 mg, 7.28 mmol) was added to a solution of 3-fluoro-4-trifluoromethyl-benzoic acid (682 mg, 3.28 mmol) and benzyl alcohol (471 mg, 4.36 mmol) in DMSO (7.3 ml), and the mixture was stirred at room temperature for 16 hours. The reaction solution was made acidic by adding concentrated hydrochloric acid, and the precipitated insoluble matter was then filtered off. The resulting solid was washed with water and then dried to give 3-benzyloxy-4-trifluoromethyl-benzoic acid as a crude compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-a639086764e34d4cbe06ae5c9e3108ea
Source noteuspto-grants-2015_10