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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 476410생성일: 2026년 10월 26일

Hydrazine, 1,1-diphenyl-, hydrochloride (1:1) → 11,12-Diphenyl-11,12-dihydroindolo[2,3-a]carbazole

https://huagongshe.com/reaction/476410

반응식

참여 물질

역할이름HCID투입량
반응물Hydrazine, 1,1-diphenyl-, hydrochloride (1:1)HCID 10738—
반응물1,2-CyclohexanedioneHCID 13006—
용매Acetic AcidHCID 176—
생성물11,12-Diphenyl-11,12-dihydroindolo[2,3-a]carbazoleHCID 2210511157.2%

반응 단계

1,2-Cyclohexadione (98%; 5.0 g, 1 eq.) is dissolved in acetic acid (100%; 30 ml). 1,1-Diphenylhydrazine hydrochloride (98%; 19.68 g, 2 eq.) is slowly added thereto. The suspension is stirred at room temperature overnight. Subsequently, the reaction is stirred at reflux for 54 h. After cooling to room temperature, the suspension is filtered with suction and washed with a little acetic acid. The residue is suspended in hot distilled water, filtered off with suction and washed to neutrality. The solid is dried under reduced pressure overnight. Subsequently, the solid is dissolved in toluene (300 ml) and Pd/C (10%; 2 g) is added; the mixture is stirred at reflux overnight. The solution was filtered through Celite (super standard) and washed with toluene and methylene chloride. The clear solution is concentrated and the residue is dried at 100° C. under reduced pressure. This gives 5.11 g of compound 4, 57.2% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637857B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-801948ef2fba41688a0b9b65b6eed340
출처 메모uspto-grants-2014_01