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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2120199생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2120199

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium CarbonateHCID 10340—
반응물Thiophene-3-boronic acidHCID 581760—
반응물6-bromo-2,3-dihydro-1H-indol-2-oneHCID 2773289—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물6-Thiophen-3-yl-1,3-dihydroindol-2-oneHCID 2343902736%

반응 조건

온도100 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06689806B1
출처 데이터셋uspto-grants-2004_02
ORD IDord-8ebbe8af7bd04340aed5ecb28d12c08f
출처 메모uspto-grants-2004_02