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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255057Generated: November 3, 2026

Ethyl alpha-oxo-4-(trifluoromethyl)benzeneacetate → Hydroxy 4-(trifluoromethyl)phenylacetic acid ethyl ester

https://huagongshe.com/reaction/1255057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl alpha-oxo-4-(trifluoromethyl)benzeneacetateHCID 2774410—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductHydroxy 4-(trifluoromethyl)phenylacetic acid ethyl esterHCID 2028679487.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2-oxo-2-(4-(trifluoromethyl)phenyl)acetate (500 mg, 2.03 mmol) is dissolved in absolute EtOH (10 mL) and cooled at 0° C. under N2. NaBH4 (38.4 mg, 1.02 mmol) is added in two portions and the resulting suspension is allowed to warm to RT and stirred for 45 minutes. The solvent is evaporated, the resulting residue is diluted with Et2O and cool water is added. The organic layer is separated, washed with water and brine, dried over Na2SO4, filtered and evaporated obtaining intermediate I149 as a colorless oil (440 mg, 87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455646B2
Source datasetuspto-grants-2013_06
ORD IDord-5929906ad77f43998a7e3967d55f1661
Source noteuspto-grants-2013_06