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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49826생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/49826

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물TriethylamineHCID 8471—
반응물Ethyl 3-aminobenzoateHCID 11400—
반응물4'-Fluoro-3'-nitroacetophenoneHCID 2734612—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Ethyl (4-acetyl-2-nitrophenyl)aminobenzoateHCID 53953856938.3%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710044B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-624de12a3733497c8932b4e4bb825d7e
출처 메모uspto-grants-2004_03