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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantHexaneHCID 8058—
ReactantN-Fluoro-4-methylpyridinium-2-sulfonateHCID 2737404—
Reactant1-(2,4-Difluorophenyl)-2-fluoro-2-(methylsulfanyl)ethanoneHCID 10632701—
Solvent1,1,2-TrichloroethaneHCID 6574—
Product2-Methylthio-2,2,2',4'-tetrafluoroacetophenoneHCID 1022034747.5%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05945438
Source datasetuspto-grants-1999_08
ORD IDord-d6b8731c671a4d33a553d33cbf793a75
Source noteuspto-grants-1999_08