Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561458Generated: November 4, 2026

2,2-Difluorocyclopropyl(4-chlorophenyl) ketone → 1-(4-Chlorophenyl)-1-(2,2-difluorocyclopropyl)ethanol

https://huagongshe.com/reaction/561458

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Difluorocyclopropyl(4-chlorophenyl) ketoneHCID 24865871—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product1-(4-Chlorophenyl)-1-(2,2-difluorocyclopropyl)ethanolHCID 58392256—

Reaction Steps

5.7 ml (17.1 mmol) of a 3N solution of methylmagnesium bromide in diethyl ether were added to 2.47 g (11.4 mmol) of the compound from Example 124A in 40 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 2.09 g (78% 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-e45977603075426dacc7046eda30898d
Source noteuspto-grants-2011_11