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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070982Generated: October 31, 2026

Dimethyl Sulfoxide → 1,1,1-Trifluoro-4-methyl-4-pyridin-2-ylpentan-2-one

https://huagongshe.com/reaction/1070982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant1,1,1-Trifluoro-4-methyl-4-pyridin-2-ylpentan-2-olHCID 22398501—
SolventDichloromethaneHCID 6344—
Product1,1,1-Trifluoro-4-methyl-4-pyridin-2-ylpentan-2-oneHCID 2239848786.5%

Reaction Steps

A solution of 516 μL (1.03 mmol, 1.2 eq) of oxalyl chloride (2.0 M solution in dichloromethane) was diluted with 2 mL of dichloromethane. To this solution was added a solution of 146 μL (2.06 mmol, 2.4 eq.) of DMSO in 0.2 mL of dichloromethane at −60° C. and the mixture was stirred for 10 minutes at this temperature. Then to this mixture was added a solution of 200 mg (0.86 mmol) of 1,1,1-trifluoro-4-methyl-4-pyridin-2-ylpentan-2-ol in 2 mL of dichloromethane at −60° C. The resulting mixture was stirred at −60° C. for 15 minutes and then 600 μL (4.3 mmol, 5.0 eq.) of triethylamine was added. The cooling bath was removed and the reaction mixture was allowed to warm to room temperature and quenched with water. The organic layer was separated. The aqueous layer was extracted three times with dichloromethane. The combined organic layers were dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by flash chromatography, providing 172 mg (86%) 1,1,1-trifluoro-4-methyl-4-pyridin-2-ylpentan-2-one as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903215B2
Source datasetuspto-grants-2005_06
ORD IDord-3ea14397c2c642968a4f118bafc7acf8
Source noteuspto-grants-2005_06