반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][C:3]=1I.[Cu](C#N)[C:14]#[N:15].C(OCC)(=O)C.CCCCCC>CN(C=O)C.[Hg]>[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][C:3]=1[C:14]#[N:15]참가 물질
반응 조건
- 온도
- 100 °C
실험 절차
In a 2-liter flask equipped with a septum inlet, magnetic stirring bar, and condenser leading to a mercury bubbler was placed 100 g (0.348 mol) of 4-amino-3-iodobenzotrifluoride in 1 liter DMF. To this reaction flask with stirring was added 37.4 g (0.416 mol) of copper cyanide and the contents were heated to 100° C. under nitrogen for fourteen hours. Afterwards, TLC analysis revealed minor starting material (20/80) ethyl acetate/hexane. The contents were cooled to 40° C. and filtered through a pad of Celite. The solids were washed with ether and the filtrate transferred to a separatory funnel and washed with about 5% aqueous ammonium hydroxide. The aqueous layer was back-extracted with ether and the organics were combined and washed with brine, dried over magnesium sulfate, filtered and concentrated to yield a black oil. The oil was chromatographed on a Biotage 75L cartridge with ethyl acetate/hexane to obtain 68 g 2-amino-5-(trifluoromethyl)benzonitrile as a black solid.
후처리
- customIn a 2-liter flask equipped with a septum inlet, magnetic stirring bar, and condenser
- temperatureThe contents were cooled to 40° C.
- filtrationfiltered through a pad of Celite
- washThe solids were washed with ether
- customthe filtrate transferred to a separatory funnel
- washwashed with about 5% aqueous ammonium hydroxide
- extractionThe aqueous layer was back-extracted with ether
- washwashed with brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto yield a black oil
- customThe oil was chromatographed on a Biotage 75L cartridge with ethyl acetate/hexane
출처 및 근거
- ORD 기록
- ord-f2cdae7306054d90a7be368476e099d5
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07737295B2
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