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HRID 1181383생성일: 2026년 10월 27일

5-(Trifluoromethyl)pyridine-2-carbonitrile → [5-(Trifluoromethyl)pyridin-2-yl]methanamine

https://huagongshe.com/reaction/1181383

반응식

참여 물질

역할이름HCID투입량
반응물5-(Trifluoromethyl)pyridine-2-carbonitrileHCID 1535372—
촉매NickelHCID 935—
용매EthanolHCID 702—
용매Ammonium HydroxideHCID 14923—
생성물[5-(Trifluoromethyl)pyridin-2-yl]methanamineHCID 379637530.5%

반응 단계

To a nitrogen flushed solution of 2-cyano-5-(trifluoromethyl)pyridine (Description 1; 8.0 g, 46.5 mmol) in a mixture of ethanol (100 ml) and ammonium hydroxide (25 ml) was added a spatula end of Raney Nickel and the resulting mixture hydrogenated at 50 psi overnight. The catalyst was removed by filtration and the filtrate was evaporated to dryness. The residue was purified by column chromatography on silica eluting with a gradient rising from 2% MeOH in dichloromethane+0.5% NH4OH to 5% MeOH in dichloromethane+0.5% NH4OH to give the title compound (2.5 g, 30%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07285563B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-8b793d41cda548b9a29289ee00b56bb1
출처 메모uspto-grants-2007_10