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HRID 17030생성일: 2026년 10월 23일

2-Iodo-4-(trifluoromethyl)aniline → 4-Amino-3-cyanobenzotrifluoride

https://huagongshe.com/ko/reaction/17030

반응식

참여 물질

역할이름HCID투입량
반응물2-Iodo-4-(trifluoromethyl)anilineHCID 2783322—
반응물Ethyl acetate hexaneHCID 21226206—
반응물HCID 178418260HCID 178418260—
촉매MercuryHCID 23931—
용매DimethylformamideHCID 6228—
생성물4-Amino-3-cyanobenzotrifluorideHCID 12627361105%

반응 조건

온도100 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737295B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f2cdae7306054d90a7be368476e099d5
출처 메모uspto-grants-2010_06