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HRID 395751作成日:2026年10月25日

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

https://huagongshe.com/reaction/395751

反応式

関与物質

役割名称HCID仕込み量
反応物N-(4-fluorophenyl)-2-nitrobenzamideHCID 691037—
反応物Sodium borohydrideHCID 4311764—
触媒Nickel acetate tetrahydrateHCID 62601—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物2-amino-N-(4-fluorophenyl)benzamideHCID 47882281%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605626B2
出典データセットuspto-grants-2003_08
ORD IDord-9ead5ee5720c457daaeaa252346062d3
出典メモuspto-grants-2003_08