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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41847Generated: October 27, 2026

Dimethyl Sulfoxide → 4,4-Difluorocyclohexanone

https://huagongshe.com/reaction/41847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant4,4-Difluorocyclohexan-1-olHCID 546300—
SolventDichloromethaneHCID 6344—
Product4,4-DifluorocyclohexanoneHCID 1578909288.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

The inside of a reactor was sufficiently dried by vacuum heating, and the atmosphere inside the reactor was replaced with dry nitrogen. The reactor was charged with 2000 ml of dichloromethane and 128.4 ml (1.5 mol) of oxalyl chloride at −78° C. After the dropwise addition of 233 ml (3.0 mol) of DMSO, the mixture was stirred at −78° C. After 10 minutes had elapsed, a dichloromethane (300 ml) solution of 136.1 g (1.0 mol) of 4,4-difluorocyclohexanol was added dropwise to the mixture using a syringe over 10 minutes. After stirring the reaction mixture at −78° C. for 40 minutes and at −45° C. for 40 minutes, N,N-diisopropylethylamine (500 ml) was added to the reaction mixture. After stirring the mixture at 0° C. for 20 minutes, a saturated ammonium chloride aqueous solution (1000 ml) was added to the mixture to terminate the reaction. The mixture was then extracted three times with dichloromethane (3000 ml). The organic layer was washed with 1N hydrochloric acid and a saturated salt solution, and dried over magnesium sulfate. After removing anhydrous magnesium sulfate using a Buchner funnel, the solvent was evaporated. The residue was distilled under reduced pressure (30 mmHg) to obtain 4,4-difluorocyclohexanone (118.9 g (yield: 85%)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08535871B2
Source datasetuspto-grants-2013_09
ORD IDord-8ddd63eebbf7424ca041fd36b7b79925
Source noteuspto-grants-2013_09