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HRID 2120199作成日:2026年10月26日

Ethanol → 6-Thiophen-3-yl-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/2120199

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium CarbonateHCID 10340—
反応物Thiophene-3-boronic acidHCID 581760—
反応物6-bromo-2,3-dihydro-1H-indol-2-oneHCID 2773289—
触媒HCID 178418397HCID 178418397—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物6-Thiophen-3-yl-1,3-dihydroindol-2-oneHCID 2343902736%

反応条件

温度100 °C

反応手順

To a warm, stirred solution of 6-bromo-2-oxindole (4 g, 26.3 mmol) dissolved in 60 mL toluene and 60 mL ethanol was added tetrakis(triphenylphosphine)palladium(0) (2.3 g, 1.9 mmol) followed by 2M aqueous sodium carbonate (50 mL, 100 mmol) and thiophene-3-boronic acid (4.3 g, 33.6 mmol). The mixture was stirred at 100° C. in an oil bath for 12 hours. The reaction mixture was cooled, diluted with ethyl acetate (500 mL), washed with IN hydrochloric acid (200 mL), water (200 mL), saturated sodium bicarbonate (200 mL) and brine (200 mL). The organic layer was separated, dried over anhydrous magnesium sulfate and concentrated to give a black solid. The solid was triturated with methylene chloride to give 2.02 g (36%) of 6-thiophen-3-yl-1,3-dihydroindol-2-one as a purple-gray solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06689806B1
出典データセットuspto-grants-2004_02
ORD IDord-8ebbe8af7bd04340aed5ecb28d12c08f
出典メモuspto-grants-2004_02