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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 654348생성일: 2026년 10월 24일

Aniline → 2-Hydroxy-N-phenyl-11H-benzo[A]carbazole-3-carboxamide

https://huagongshe.com/ko/reaction/654348

반응식

참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물Phenyl2-hydroxy-11H-benzo[a]carbazole-3-carboxylateHCID 19933809—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-Hydroxy-N-phenyl-11H-benzo[A]carbazole-3-carboxamideHCID 15596992166.2%

반응 단계

The phenyl 2-hydroxy-11H-benzo(a)carbazole-3-carboxylate obtained from Example I (5 grams, 14 millimoles), aniline (2.75 grams, 28 millimoles) and 15 milliliters of N-methyl pyrrolidinone were charged in a 100 milliliter 3-neck flask equipped with a magnetic stirrer and a nitrogen inlet. The resulting mixture was stirred and was heated to reflux at an oil bath temperature of ~250° C. under a nitrogen atmosphere. After 3 hours, TLC analysis revealed that all the starting phenyl ester was consumed. The mixture was cooled to room temperature and was poured into a 1 liter beaker containing 400 milliliters of ice cold 5 percent of HCl. The yellow precipitate obtained was isolated by filtration. After washing with water (~200 milliliters) and ~20 milliliters of methanol and vacuum drying, 4.7 grams of crude product resulted. This product was then recrystallized from a mixture of (dimethylformamide) DMF/MeOH/H2O (~30 milliliter each) yielding 4.1 grams (83 percent) of 2-hydroxy-11H-benzo(a)carbazole-3-carboxanilide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05130443
출처 데이터셋uspto-grants-1992_07
ORD IDord-e182c9a22cc24161b9e73f13b2aeca9b
출처 메모uspto-grants-1992_07