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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561456Generated: November 1, 2026

2-[4-(Trifluoromethyl)benzoyl]cyclopropanecarbonitrile → 2-{1-Hydroxy-1-[4-(trifluoromethyl)phenyl]ethyl}cyclopropanecarbonitrile

https://huagongshe.com/reaction/561456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[4-(Trifluoromethyl)benzoyl]cyclopropanecarbonitrileHCID 58392093—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product2-{1-Hydroxy-1-[4-(trifluoromethyl)phenyl]ethyl}cyclopropanecarbonitrileHCID 58392511—

Reaction Steps

3.0 ml (9.09 mmol) of a 3N solution of methylmagnesium bromide in diethyl ether were added to 1.45 g (6.06 mmol) of the compound from Example 122A in 25 ml of diethyl ether at RT, and the mixture was stirred at RT overnight. The reaction mixture was added to a saturated, ice-cold aqueous ammonium chloride solution, the phases were separated, the aqueous phase was extracted with dichloromethane, and the combined organic phases were dried over magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography on silica gel (mobile phase: toluene/ethyl acetate gradient) to result in 1.40 g (90% 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-1c2c57ba6943470a95f88ed490a8d2b3
Source noteuspto-grants-2011_11