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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1586434생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1586434

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참여 물질

역할이름HCID투입량
반응물ChloroformHCID 6212—
반응물HexaneHCID 8058—
반응물Pyridinium, 1-fluoro-, 1,1,1-trifluoromethanesulfonate (1:1)HCID 2724576—
반응물1-(2,4-Difluorophenyl)-2-(methylsulfanyl)ethan-1-oneHCID 10655717—
용매1,1,2-TrichloroethaneHCID 6574—
생성물2-Methylthio-2,2,2',4'-tetrafluoroacetophenoneHCID 1022034747%

반응 조건

온도100 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05945438
출처 데이터셋uspto-grants-1999_08
ORD IDord-7ee50cf0d8fe4cadba3e9d4c1d1dd879
출처 메모uspto-grants-1999_08