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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74173생성일: 2026년 10월 23일

2-Aminophenol → 4-fluoro-N-(2-hydroxyphenyl)-3-nitrobenzanilide

https://huagongshe.com/ko/reaction/74173

반응식

참여 물질

역할이름HCID투입량
반응물2-AminophenolHCID 5801—
반응물ChloroformHCID 6212—
반응물TriethylamineHCID 8471—
반응물4-Fluoro-3-nitrobenzoic acidHCID 67987—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
용매Ethyl AcetateHCID 8857—
생성물4-fluoro-N-(2-hydroxyphenyl)-3-nitrobenzanilideHCID 6749793468%

반응 단계

To a solution of 4-fluoro-3-nitrobenzoic acid (2.00 g, 10.8 mmol) in chloroform (40 mL) was added 2-aminophenol (1.18 g, 10.8 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (2.17 g, 11.3 mmol), and triethylamine (1.15 g, 11.3 mmol), and this was stirred at room temperature for 2.5 hours. After the reaction was complete, this was diluted by adding ethyl acetate, and this was washed with water, 1N hydrochloric acid, and saturated aqueous sodium hydrogen carbonate. The organic layer obtained was dried over anhydrous sodium sulfate, after which it was filtered and concentrated to yield the title compound (2.02 g, 68% yield) as orange crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e51a015c6d30428c8a4b915518a238cb
출처 메모uspto-grants-2014_09