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HRID 2360489作成日:2026年10月26日

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

https://huagongshe.com/reaction/2360489

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl pyruvateHCID 12041—
反応物(2-Bromophenyl)hydrazineHCID 85583—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物Ethyl 7-bromo-1H-indole-2-carboxylateHCID 7017885—

反応条件

温度40 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08686022B2
出典データセットuspto-grants-2014_04
ORD IDord-06ccfba4493d41d8970d228e872606e7
出典メモuspto-grants-2014_04