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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561488Generated: November 1, 2026

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

https://huagongshe.com/reaction/561488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant2-[2-Fluoro-4-(trifluoromethyl)benzoyl]cyclopropanecarbonitrileHCID 58392283—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2-{[2-Fluoro-4-(trifluoromethyl)phenyl] (hydroxy)methyl}cyclopropanecarbonitrileHCID 58392135—

Reaction Conditions

Temperature40 °C

Reaction Steps

351 mg (9.28 mmol) of sodium borohydride were added to 2.17 g (8.44 mmol) of the compound from Example 129A in 38 ml of ethanol and 16 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 9/1) to result in 1.59 g (73% 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-acb835598e0c48a2ba7be3a9cc14c270
Source noteuspto-grants-2011_11