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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 557168생성일: 2026년 10월 26일

Water → 7-Ethenyl-1H-indole

https://huagongshe.com/reaction/557168

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TributylvinyltinHCID 81998—
반응물Lithium ChlorideHCID 433294—
반응물7-BromoindoleHCID 2757020—
촉매TriphenylphosphineHCID 11776—
촉매HCID 178479785HCID 178479785—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물7-Ethenyl-1H-indoleHCID 1456740480%

반응 조건

온도100 °C

반응 단계

Add tributyl(vinyl)tin (9.8 mL, 33.7 mmol), triphenyl-phosphine (0.4 g, 1.53 mmol), diphenylpalladium(II) dichloride (1.07 g, 1.53 mmol) and lithium chloride (4.0 g, 94.4 mmol) to 7-bromo-1H-indole (6.0 g, 30.6 mmol) in 150 mL of dimethylformamide and heat the resulting mixture at 100° C. overnight. Cool the reaction mixture to 20-24° C. and poured into a mixture of 150 mL of water and 150 mL of ethyl acetate. Wash the aqueous layer with additional ethyl acetate (3×100 mL), combine the organic layers, wash with saturated aqueous sodium chloride, dry over magnesium sulfate, filter, and concentrate under reduced pressure. Subject the residue to silica gel chromatography, eluting with 5-10% ethyl acetate in hexanes. Combine fractions containing product and concentrate them under reduced pressure to provide the desired compound as a clear oil (3.5 g, 80%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08058425B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-968e909d4d174403abf46155922e6b3a
출처 메모uspto-grants-2011_11