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HRID 49826作成日:2026年10月26日

Ethanol → Ethyl (4-acetyl-2-nitrophenyl)aminobenzoate

https://huagongshe.com/reaction/49826

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物TriethylamineHCID 8471—
反応物Ethyl 3-aminobenzoateHCID 11400—
反応物4'-Fluoro-3'-nitroacetophenoneHCID 2734612—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物Ethyl (4-acetyl-2-nitrophenyl)aminobenzoateHCID 53953856938.3%

反応手順

A mixture 1b (11.0 g, 60.2 mmol), ethyl 3-aminobenzoate (9.9 g, 6.2 mmol) and triethylamine (8.34 ml, 60.2 mmol) in anhydrous NMP (5 ml) was heated to 130° C. with stirring under a stream of nitrogen for 4 hours. The cooled mixture was poured into ice-water (100 ml). Ethanol (10 ml) was added and the mixture was stirred until crystallization was completed. The precipitate was filtered off, washed with water and dried to yield ethyl (4-acetyl-2-nitrophenyl)aminobenzoate (19.1 g, 97%). This ester was hydrogenated quantitatively in a mixture of ethanol (400 ml) and dichloromethane (100 ml) using Pd (5% on activated carbon) as the catalyst. The resulting diamine was heated to reflux in formic acid (100 ml) for 1 hour. The cooled mixture was poured into ice-water (400 ml) and the precipitate was filtered off, washed with water and dried to yield 5-acetyl-1-(3-ethoxycarbonyl)phenylbenzimidazole (16.4 g, 91%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710044B2
出典データセットuspto-grants-2004_03
ORD IDord-624de12a3733497c8932b4e4bb825d7e
出典メモuspto-grants-2004_03