Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 523248생성일: 2026년 10월 26일
Acetic Acid → 5-bromo-2-(ethoxycarbonyl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid
https://huagongshe.com/reaction/523248
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Ethyl 3-oxocyclohexanecarboxylate | HCID 118096 | — |
| 반응물 | 4-Bromo-2-hydrazinyl-5-methylbenzoic acid hydrochloride | HCID 117761019 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 5-bromo-2-(ethoxycarbonyl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid | HCID 117775453 | 55% |
반응 단계
A mixture of 4-bromo-2-hydrazinyl-5-methylbenzoic acid hydrochloride (2.17 g, 7.71 mmol), ethyl 3-oxocyclohexanecarboxylate (1.44 g, 8.48 mmol) and acetic acid (1.32 mL, 23.1 mmol) in toluene (40 mL) was heated in an oil bath at 117° C. for 5 h. The mixture was concentrated and dried under vacuum, and the residue was diluted with toluene (18 mL) and TFA (4.5 mL). The mixture was heated at 90° C. overnight. The cooled mixture was diluted with EtOAc, sonicated, and the precipitate was collected by filtration and washed with EtOAc to give a yellow solid. The filtrate was concentrated and the residue was suspended in EtOAc with sonication. The precipitate was collected by filtration and combined with the first precipitate. The solid was triturated with MeOH to give 5-bromo-2-(ethoxycarbonyl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acid as a pale yellow solid (1.60 g, 55% yield). Mass spectrum m/z 380, 382 (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-3757c9ebbabb4d82bc41aa9394744026 |
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| 출처 메모 | uspto-grants-2016_05 |
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