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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611814Generated: October 26, 2026

Chloroform → 2-Methylthio-2,2,2',4'-tetrafluoroacetophenone

https://huagongshe.com/reaction/611814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantHexaneHCID 8058—
ReactantPyridinium, 1-fluoro-, 1,1,1-trifluoromethanesulfonate (1:1)HCID 2724576—
Reactant1-(2,4-Difluorophenyl)-2-(methylsulfanyl)ethan-1-oneHCID 10655717—
Solvent1,1,2-TrichloroethaneHCID 6574—
Product2-Methylthio-2,2,2',4'-tetrafluoroacetophenoneHCID 1022034747%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a 20 ml solution of 0.5 g (2.5 mmol) of 2',4'-difluoro-2-(methylthio)acetophenone [Compound (2a-1)] in 1,1,2-trichloroethane, 3.0 g (12.1 mmol) of N-fluoropyridinium triflate ("Onoda Fluorinate FP-T500", trade name; product of Chichibu Onoda Co., Ltd.) were added at an internal temperature of 80° C., followed by stirring at an internal temperature of 100° C. for one hour. After cooling, the reaction mixture was added to n-hexane. The insoluble matter 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 distilled off under reduced pressure. The residue so obtained was subjected to chromatography on a silica gel column using chloroform, whereby 0.28 g of the title Compound (2c-1) was obtained in the form of a light yellow oil (yield: 47.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06002028
Source datasetuspto-grants-1999_12
ORD IDord-f4f2b2c86ea24ca3955ffb27685c1d7c
Source noteuspto-grants-1999_12