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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2360489생성일: 2026년 10월 26일

Water → Ethyl 7-bromo-1H-indole-2-carboxylate

https://huagongshe.com/reaction/2360489

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethyl pyruvateHCID 12041—
반응물(2-Bromophenyl)hydrazineHCID 85583—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 7-bromo-1H-indole-2-carboxylateHCID 7017885—

반응 조건

온도40 °C

반응 단계

11.0 g 2-bromophenylhydrazine and 550 mg p-toluenesulphonic acid monohydrate are dissolved in 200 ml of toluene, combined with 6.74 ml ethyl pyruvate and refluxed for 2 hours using the water separator. The mixture is allowed to cool to 40° C. and combined with a solution that is obtained by dissolving 44.75 g p-toluenesulphonic acid monohydrate in 300 ml of toluene and refluxing for two hours using the water separator. Then the mixture is refluxed for 12 hours using the water separator. After cooling to ambient temperature the solvents are eliminated in vacuo, the residue is taken up in ethyl acetate and washed successively with water and saturated aqueous sodium hydrogen carbonate solution. After drying with magnesium sulphate the mixture is combined with activated charcoal, stirred for 15 minutes and filtered through kieselguhr. The process of adding activated charcoal, stirring and filtering is repeated twice more. The solvents are eliminated in vacuo and the residue is taken up in petroleum ether/dichloromethane 7:3. 30 g of silica gel are added, the mixture is stirred for 10 minutes and then suction filtered through kieselguhr. The suction filtered silica gel is washed with petroleum ether/dichloromethane 7:3. The solvents are eliminated in vacuo.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08686022B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-06ccfba4493d41d8970d228e872606e7
출처 메모uspto-grants-2014_04