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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24405생성일: 2026년 10월 24일

Water → 3-(4,5,2'-Trimethoxybiphenyl-2-ylmethylene)-1,3-dihydroindol-2-one

https://huagongshe.com/ko/reaction/24405

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium CarbonateHCID 10340—
반응물2-Methoxyphenylboronic acidHCID 2733958—
반응물3-(3-Bromo-4,5-dimethoxybenzylidene)-1,3-dihydroindol-2-oneHCID 54564604—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물3-(4,5,2'-Trimethoxybiphenyl-2-ylmethylene)-1,3-dihydroindol-2-oneHCID 5420975764.5%

반응 단계

Tetrakis(triphenylphosphine)palladium(0) (0.02 g, 0.02 mmol) was added to a solution of 3-(3-bromo-4,5-dimethoxybenzylidene)-1,3-dihydroindol-2-one (0.20 g, 0.56 mmol) in toluene (1 ml) and ethanol (1 ml), followed by addition of 2M aqueous sodium carbonate (1.1 ml, 2.2 mmol). To this mixture was added 2-methoxyphenylboronic acid (0.09 g, 0.62 mmol), and the mixture was held at 100° C. in a sealed tube for 12 hours. The reaction mixture was added to 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). The organic layer was dried over magnesium sulfate and concentrated. Chromatography (silica, 30-40% ethyl acetate/hexanes) afforded 0.14 g (64%) of 3-(4,5,2′-trimethoxy-biphenyl-2-ylmethylene)-1,3-dihydroindol-2-one as an orange solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-23766819bdb742cc8acaacd93b4c925c
출처 메모uspto-grants-2005_02