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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351576생성일: 2026년 10월 25일

Water → 7-Ethenyl-1H-indole

https://huagongshe.com/reaction/351576

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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%

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온도100 °C

반응 단계

To 7-bromo-1H-indole (6.0 g, 30.6 mmol) in 150 mL of dimethylformamide was added tributyl(vinyl)tin (9.8 mL, 33.7 mmol), triphenylphosphine (0.4 g, 1.53 mmol), diphenyl-palladium(II) dichloride (1.07 g, 1.53 mmol) and lithium chloride (4.0 g, 94.4 mmol), and the resulting mixture was heated at 100° C. overnight. The reaction mixture was cooled to 20-24° C. and poured into 150 mL of water and 150 mL of ethyl acetate. The aqueous layer was washed with additional ethyl acetate (3×100 mL) and the combined organic layers were washed with saturated aqueous sodium chloride, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 5-10% ethyl acetate in hexanes. Fractions containing product were combined and concentrated under reduced pressure to provide 3.5 g (80%) of the desired compound as a clear oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743785B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-0cfbd83475514974a0e7c40b96b6fc3f
출처 메모uspto-grants-2004_06