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HRID 1603285作成日:2026年10月26日

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

https://huagongshe.com/reaction/1603285

反応式

関与物質

役割名称HCID仕込み量
反応物ChloroformHCID 6212—
反応物HexaneHCID 8058—
反応物N-Fluoro-4-methylpyridinium-2-sulfonateHCID 2737404—
反応物1-(2,4-Difluorophenyl)-2-fluoro-2-(methylsulfanyl)ethanoneHCID 10632701—
溶媒1,1,2-TrichloroethaneHCID 6574—
生成物2-Methylthio-2,2,2',4'-tetrafluoroacetophenoneHCID 1022034747.5%

反応条件

温度100 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05986144
出典データセットuspto-grants-1999_11
ORD IDord-9ff763c582c047de971aa0222fe2b9e3
出典メモuspto-grants-1999_11