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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810308Generated: November 1, 2026

Benzyl Alcohol → (3-Benzyloxy-5-trifluoromethyl-phenyl)-acetic acid

https://huagongshe.com/reaction/1810308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium hydrideHCID 24758—
Reactant3-Fluoro-5-(trifluoromethyl)phenylacetic acidHCID 2759172—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(3-Benzyloxy-5-trifluoromethyl-phenyl)-acetic acidHCID 59644613—

Reaction Conditions

Temperature120 °C

Reaction Steps

To 3-fluoro-5-(trifluoromethyl)phenylacetic acid (2.0 g, 9.0 mmol) and benzyl alcohol (1.9 mL, 18.0 mmol) in NMP (10 mL) was added sodium hydride (60% in mineral oil; 0.8 g, 19.8 mmol), and the reaction was stirred at 120° C. for 3 hours. The mixture was acidified and extracted with EtOAc, and the crude material was purified by silica gel chromatography to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362044B2
Source datasetuspto-grants-2013_01
ORD IDord-2f953c3c988b41f88870239a3573e9fa
Source noteuspto-grants-2013_01