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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1586435Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1586435

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
Edukt1-Fluoro-2,4,6-trimethylpyridinium Trifluoromethanesulfonate [Fluorinating Reagent]HCID 2724575—
Edukt1-(2,4-Difluorophenyl)-2-(methylsulfanyl)ethan-1-oneHCID 10655717—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt1-(2,4-Difluorophenyl)-2-fluoro-2-(methylsulfanyl)ethanoneHCID 1063270190,8%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05945438
Quelldatensatzuspto-grants-1999_08
ORD IDord-3a69dbae840e407bae08bc03f46c1a33
Quellennotizuspto-grants-1999_08