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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1860791생성일: 2026년 10월 27일

Water → 3-(4-Methoxy-3-thiophen-3-ylbenzylidene)-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/1860791

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium CarbonateHCID 10340—
반응물Thiophene-3-boronic acidHCID 581760—
반응물3-(3-Bromo-4-methoxybenzylidene)-1,3-dihydroindol-2-oneHCID 2803107—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물3-(4-Methoxy-3-thiophen-3-ylbenzylidene)-1,3-dihydroindol-2-oneHCID 5370652050%

반응 단계

Tetrakis(triphenylphosphine)palladium(0) (0.02 g, 0.02 mmol) was added to a solution of 3-(3-bromo-4-methoxybenzylidene)-1,3-dihydroindol-2-one (0.2 g, 0.61 mmol) in toluene (1 ml) and ethanol (1 ml), followed by addition of 2M aqueous sodium carbonate (1.2 ml, 2.4 mmol). To this mixture was added thiophene-3-boronic acid (0.09 g, 0.67 mmol) and the mixture was held at 100° C. in a sealed tube for 12 hours. The reaction was then poured into water (50 ml) and extracted with ethyl acetate (2×100 ml). The combined organic layers were washed with saturated aqueous sodium bicarbonate (50 ml) and brine (50 ml), dried over magnesium sulfate and concentrated. Chromatography (silica, methylene chloride then 30-40% ethyl acetate/hexanes) afforded 0.1 g (50%) of 3-(4-methoxy-3-thiophen-3-ylbenzylidene)-1,3-dihydroindol-2-one as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06531502B1
출처 데이터셋uspto-grants-2003_03
ORD IDord-b187382ae0ef4d0fa4da8c4fffe5ef2d
출처 메모uspto-grants-2003_03