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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49017생성일: 2026년 10월 24일

O-Phenylenediamine → 4-[3-(2-{1-[4-Carboxyphenyl]-ethylamino}-phenyl)-ureido]-benzonitrile

https://huagongshe.com/ko/reaction/49017

반응식

참여 물질

역할이름HCID투입량
반응물O-PhenylenediamineHCID 7243—
반응물Potassium CarbonateHCID 11430—
반응물4-Cyanophenyl isocyanateHCID 170380—
반응물4-(1-Bromoethyl)benzoic acidHCID 5146225—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물4-[3-(2-{1-[4-Carboxyphenyl]-ethylamino}-phenyl)-ureido]-benzonitrileHCID 20635143—

반응 단계

12.8 g (88.8 mmol) 4-cyanophenylisocyanat were dissolved in 500 ml diethyl ether at rt. 9.6 g (88.8 mmol) o-phenylene diamine were added with stirring. After stirring overnight, the reaction mixture was filtrated and the solid washed with diethylether. The so prepared mono-urea derivative was sufficient pure for further reactions. 3.78 (15 mmol) were dissolved in 30 ml anhydrous dry DMF, 3.44 g (15 mmol) 4-(1-bromoethyl)-benzoic acid and 2 g potassium carbonate were added and stirred for 3 days at rt. The solvent was removed under reduced pressure, the product dissolved in ethyl acetate and extracted with 1 m HCl, water and brine. The organic phase was dried over sodium sulfate and the solvent removed under reduced pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706715B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-5171a0f3ec00423cbedc952e18e7cb9a
출처 메모uspto-grants-2004_03