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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603284Generated: October 25, 2026

Hexane → 1-(2,4-Difluorophenyl)-2-fluoro-2-(methylsulfanyl)ethanone

https://huagongshe.com/reaction/1603284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1-Fluoro-2,4,6-trimethylpyridinium Trifluoromethanesulfonate [Fluorinating Reagent]HCID 2724575—
Reactant1-(2,4-Difluorophenyl)-2-(methylsulfanyl)ethan-1-oneHCID 10655717—
Solvent1,2-DichloroethaneHCID 11—
Product1-(2,4-Difluorophenyl)-2-fluoro-2-(methylsulfanyl)ethanoneHCID 1063270190.8%

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 1,2-dichloroethane, 1.1 g (3.8 mmol) of N-fluoro-2,4,6-trimethylpyridinium triflate ("Onoda Florinate FP-T300", trade name; product of Chichibu Onoda Co., Ltd.) were added at room temperature, followed by stirring at the same temperature for 12 hours. 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, whereby 0.50 g of the title Compound (2b-1) was obtained in the form of a light yellow oil (yield: 91.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05986144
Source datasetuspto-grants-1999_11
ORD IDord-ab5ec0f149d14569bb46c3ee35dcdcbf
Source noteuspto-grants-1999_11