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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561484Generated: October 31, 2026

Ammonium Chloride → 2-{Hydroxy[4-(trifluoromethyl)phenyl]methyl}cyclopropanecarbonitrile

https://huagongshe.com/reaction/561484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant2-[4-(Trifluoromethyl)benzoyl]cyclopropanecarbonitrileHCID 58392093—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2-{Hydroxy[4-(trifluoromethyl)phenyl]methyl}cyclopropanecarbonitrileHCID 58392408—

Reaction Conditions

Temperature40 °C

Reaction Steps

298 mg (7.88 mmol) of sodium borohydride were added to 1.71 g (7.17 mmol) of the compound from Example 122A in 30 ml of ethanol and 7 ml of ethyl acetate under argon, and the mixture was stirred at 40° C. for 1 h. The reaction mixture was added to saturated aqueous ammonium chloride solution and ethyl acetate, the phases were separated, the aqueous phase was extracted twice with ethyl acetate, and the combined organic phases were dried over magnesium sulfate, filtered and concentrated. The crude product was purified by flash chromatography on silica gel (mobile phase: toluene/ethyl acetate gradient) to result in 1.64 g (95% of theory) of a mixture of the diastereomers of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063234B2
Source datasetuspto-grants-2011_11
ORD IDord-324117239c8f4f05bd089775e9e08d38
Source noteuspto-grants-2011_11