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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578556Generated: October 25, 2026

Acetone → 1-((Trifluoromethyl)thio)-2-propanone

https://huagongshe.com/reaction/1578556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantEthanolHCID 702—
ReactantMethanesulfenyl chloride, trifluoro-HCID 67900—
SolventDichloromethaneHCID 6344—
Product1-((Trifluoromethyl)thio)-2-propanoneHCID 1377831269%

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 2-propanone (0.25 mole), ethanol (0.49) and dichloromethane (75 ml) was introduced into a sealed and pressure tested vessel having a volume of about 500 ml under reduced pressure. Trifluoromethanesulfenyl chloride (0.22 mole) was then added to the cooled, evacuated vessel. The vessel was warmed to about 25°C and then rocked for five days. The vessel was vented through a cold gas trap (-78°C) to trap any unreacted trifluoromethylsulfenyl chloride gas and then through a scrubbing system to remove the vented hydrogen chloride gas. Residual liquid was transferred to a flask and distilled to give about 24 g of 1-trifluoromethylthio-2-propanone. The structure of the purified product (b.p. 51°-52°C/22 mm Hg) was confirmed by spectral and elemental analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03937738
Source datasetuspto-grants-1976_02
ORD IDord-25ba989268a746fcb747b690c8fdbfa4
Source noteuspto-grants-1976_02