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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 427646생성일: 2026년 10월 24일

Chloride → N1-(4-Methoxybenzoyl)-N2-(4-ethoxybenzoyl)-1,2-benzenediamine

https://huagongshe.com/ko/reaction/427646

반응식

참여 물질

역할이름HCID투입량
반응물ChlorideHCID 312—
반응물TriethylamineHCID 8471—
반응물4-Ethoxybenzoic acidHCID 12093—
반응물N-(2-Aminophenyl)-4-methoxybenzamideHCID 785232—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N1-(4-Methoxybenzoyl)-N2-(4-ethoxybenzoyl)-1,2-benzenediamineHCID 1071542641%

반응 조건

온도0 °C

반응 단계

To a mixture of 4-ethoxybenzoic acid (0.332 g, 2.00 mmol) and a few drops of N,N-dimethylformamide in methylene chloride (50 mL) cooled to 0° C. was added oxayl chloride (0.21 mL, 2.2 mmole). After 30 min reaction the mixture was warmed to room temperature and stirred for an additional 10 min. The mixture was concentrated in vacuo, and the residue dissolved in methylene chloride (10 mL), and the resulting solution added in two portions to a mixture of N1-(4-methoxybenzoyl)-1,2-benzenediamine (0.455 g, 2.00 mmol) and triethylamine (0.281 mL, 2.00 mmol) in methylene chloride (40 mL) cooled to 0° C. After 4 h, the mixture was allowed to warm to room temperature and stirred for an additional 12 h. The reaction was quenched with cold dilute aqueous hydrochloric acid (50 mL), diluted with hexane, and shaken in a separatory funnel. The organic layer was washed with cold dilute aqueous hydrochloric acid and saturated aqueous sodium bicarbonate solution. The solution was dried (magnesium sulfate), filtered, and concentrated in vacuo. Recrystallization of the residue from methylene chloride/hexane provided 317 mg (41%) of title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313122B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-08e379e53abf4de8ab04dac4a76d590b
출처 메모uspto-grants-2001_11