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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

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Ethyl 3-oxocyclohexanecarboxylateHCID 118096—
반응물4-Bromo-2-hydrazinyl-5-methylbenzoic acid hydrochlorideHCID 117761019—
용매TolueneHCID 1140—
생성물5-bromo-2-(ethoxycarbonyl)-6-methyl-2,3,4,9-tetrahydro-1H-carbazole-8-carboxylic acidHCID 11777545355%

반응 조건

온도117 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334290B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-3757c9ebbabb4d82bc41aa9394744026
출처 메모uspto-grants-2016_05