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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Ethyl 3-oxocyclohexanecarboxylate | HCID 118096 | — |
| 반응물 | 4-Bromo-5-fluoro-2-hydrazinylbenzoic acid hydrochloride | HCID 76848196 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-bromo-7-ethoxycarbonyl-3-fluoro-6,7,8,9-tetrahydro-5H-carbazole-1-carboxylic acid | HCID 117760806 | 46.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09334290B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-ab14656f324b414d845b88d78f516f8e |
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| 출처 메모 | uspto-grants-2016_05 |
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