참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Iodo-4-(trifluoromethyl)aniline | HCID 2783322 | — |
| 반응물 | Ethyl acetate hexane | HCID 21226206 | — |
| 반응물 | HCID 178418260 | HCID 178418260 | — |
| 촉매 | Mercury | HCID 23931 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-Amino-3-cyanobenzotrifluoride | HCID 12627361 | 105% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737295B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-f2cdae7306054d90a7be368476e099d5 |
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| 출처 메모 | uspto-grants-2010_06 |
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