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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 523236생성일: 2026년 10월 25일

Acetic Acid → 4-bromo-7-ethoxycarbonyl-3-fluoro-6,7,8,9-tetrahydro-5H-carbazole-1-carboxylic acid

https://huagongshe.com/reaction/523236

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참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Ethyl 3-oxocyclohexanecarboxylateHCID 118096—
반응물4-Bromo-5-fluoro-2-hydrazinylbenzoic acid hydrochlorideHCID 76848196—
용매TolueneHCID 1140—
생성물4-bromo-7-ethoxycarbonyl-3-fluoro-6,7,8,9-tetrahydro-5H-carbazole-1-carboxylic acidHCID 11776080646.8%

반응 조건

온도110 °C

반응 단계

A mixture of 4-bromo-5-fluoro-2-hydrazinylbenzoic acid hydrochloride (5.37 g, 18.8 mmol), ethyl 3-oxocyclohexanecarboxylate (3.52 g, 20.7 mmol) and acetic acid (3.23 mL, 56.4 mmol) in toluene (90 mL) was heated at 110° C. for 20 h. The solvent was removed under reduced pressure, and the residue was diluted with toluene (43 mL) and trifluoroacetic acid (11 mL). The mixture was stirred at 90-94° C. overnight. The cooled mixture was diluted with EtOAc, sonicated, and the precipitate was collected by filtration. The filtrate was concentrated and resuspended in EtOAc with sonication, resulting in another precipitate which was also collected by filtration and washed with EtOAc. The combined solids were triturated twice with MeOH to give a solid. The combined filtrates were concentrated and the residue was triturated with MeOH to give additional solid. The solids were combined to give 5-bromo-2-ethoxycarbonyl-6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid as a pale yellow solid (3.38 g). Mass spectrum m/z 384, 386 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334290B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-ab14656f324b414d845b88d78f516f8e
출처 메모uspto-grants-2016_05