HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578556Generated: October 25, 2026
Acetone → 1-((Trifluoromethyl)thio)-2-propanone
https://huagongshe.com/reaction/1578556
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanesulfenyl chloride, trifluoro- | HCID 67900 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-((Trifluoromethyl)thio)-2-propanone | HCID 13778312 | 69% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03937738 |
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| Source dataset | uspto-grants-1976_02 |
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| ORD ID | ord-25ba989268a746fcb747b690c8fdbfa4 |
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| Source note | uspto-grants-1976_02 |
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