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HRID 654347생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/654347

반응식

참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물Phenyl2-hydroxy-11H-benzo[a]carbazole-3-carboxylateHCID 19933809—
생성물2-Hydroxy-N-phenyl-11H-benzo[A]carbazole-3-carboxamideHCID 15596992—

반응 조건

온도25 °C

반응 단계

The aromatic ester is reacted with an aniline in a solvent and heating to form the anilide product. The reaction temperature can be varied to from about 140° C. to about 280° C. or above. Specifically, phenyl 2-hydroxy-11H-benzo(a)carbazole-3-carboxylate can be reacted with aniline in methyl N-pyrrolidinone at about 250° C. The ratio of the phenyl ester to aniline can vary, for example, from about 1:1 equivalent and up to about 20 equivalents. After the reaction is completed, the product mixture is cooled to room temperature, about 25° C., and discharged into an acidic aqueous solution, such as a 5 percent HCl ice cold solution. The precipitated anilide product, such as 2-hydroxy-11H-benzo(a)carbazole-3-carboxanilide, is isolated by filtration and washed with water and methanol. Purification can be accomplished by first dissolving the crude product in a hot solvent, such as DMF, and then precipitating the product by adding water or methanol, or a mixture of methanol and water. The purified product is then characterized by melting point, IR, mass spectrometry, NMR spectroscopy, especially 13C NMR as well as elemental analysis.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05130443
출처 데이터셋uspto-grants-1992_07
ORD IDord-5dad97ebca7d4ec59c9dc23aec51fe7d
출처 메모uspto-grants-1992_07