HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586436Generated: October 26, 2026
Chloroform → 2-Methylthio-2,2,2',4'-tetrafluoroacetophenone
https://huagongshe.com/reaction/1586436
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | N-Fluoro-4-methylpyridinium-2-sulfonate | HCID 2737404 | — |
| Reactant | 1-(2,4-Difluorophenyl)-2-fluoro-2-(methylsulfanyl)ethanone | HCID 10632701 | — |
| Solvent | 1,1,2-Trichloroethane | HCID 6574 | — |
| Product | 2-Methylthio-2,2,2',4'-tetrafluoroacetophenone | HCID 10220347 | 47.5% |
Reaction Steps
In a 20 ml solution of 0.5 g (2.3 mmol) of 2-methylthio-2,2',4'-trifluoroacetophenone [Compound (2b-1)] in 1,1,2-trichloroethane, 0.7 g (3.7 mmol) of N-fluoro-4-methylpyridinium-2-sulfonate ("MEC-02", trade name; Daikin Industries, Ltd.) was added at an internal temperature of 80° C., followed by stirring at an internal temperature of 100° C. for 20 minutes. After cooling, the reaction mixture was added to n-hexane. The insoluble matter so precipitated was filtered off. The insoluble matter was then washed with ethyl ether, followed by combination with the hexane layer. The layers so combined were washed successively with water and saturated saline, followed by drying over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure. The residue so obtained was subjected to chromatography on a silica gel column using chloroform, whereby 0.26 g of the title Compound (2c-1) was obtained in the form of a light yellow oil (yield: 48.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05945438 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-d6b8731c671a4d33a553d33cbf793a75 |
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| Source note | uspto-grants-1999_08 |
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