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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023469Generated: October 26, 2026

Dimethyl Sulfoxide → 2-(4-Fluorophenyl)cyclohexan-1-one

https://huagongshe.com/reaction/1023469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 20487437HCID 20487437—
SolventDichloromethaneHCID 6344—
Product2-(4-Fluorophenyl)cyclohexan-1-oneHCID 1308954069.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of oxalyl chloride (0.45 mL, 5.2 mmol) in dry dichloromethane (15 mL) at −78° C. is added a solution of DMSO (0.73 mL, 10.3 mmol) in dichloromethane (10 mL) dropwise, and the resulting mixture is allowed to stir at −78° C. for 30 minutes. Then a solution of 2-(4-Fluoro-phenyl)-cyclohexanol (500 mg, 2.57 mmol) in dichloromethane (5 mL) is added and stirred for 15 minutes. Then triethylamine (2.87 mL, 15.4 mmol) is added and the reaction is allowed to slowly warm up to 20° C. and stirred for 16 hours. The mixture is poured into ice-water (30 mL) and organic layer is washed with water (10 mL×5), then brine (10 mL×1) and dried over anhdrous sodium sulfate. After concentration, the crude is purified by silica flash column chromatography using EtOAc in Heptane (gradient from 0% to 30%) to give 342 mg of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722709B2
Source datasetuspto-grants-2014_05
ORD IDord-c512da44ff1a4f44953c783a1409dfd6
Source noteuspto-grants-2014_05