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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395751생성일: 2026년 10월 24일

N-(4-fluorophenyl)-2-nitrobenzamide → 2-amino-N-(4-fluorophenyl)benzamide

https://huagongshe.com/ko/reaction/395751

반응식

참여 물질

역할이름HCID투입량
반응물N-(4-fluorophenyl)-2-nitrobenzamideHCID 691037—
반응물Sodium borohydrideHCID 4311764—
촉매Nickel acetate tetrahydrateHCID 62601—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물2-amino-N-(4-fluorophenyl)benzamideHCID 47882281%

반응 단계

To a stirred solution of N-(4-fluorophenyl)-2-nitrobenzamide (4.0 g, 15.4 mmol) in methanol (220 mL) and tetrahydrofuran (110 mL) was added nickel acetate tetrahydrate (7.7 g, 31 mmol). Sodium borohydride (2.3 g, 62 mmol) was added in small portions. After gas evolution had ceased, the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and concentrated ammonium hydroxide, and the layers were separated. The organic phase was washed with concentrated ammonium hydroxide and saturated aqueous sodium chloride solution, dried (magnesium sulfate), filtered, and concentrated in vacuo to give 2.86 g (81%) of the title compound as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06605626B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-9ead5ee5720c457daaeaa252346062d3
출처 메모uspto-grants-2003_08