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HRID 351576作成日:2026年10月26日

Water → 7-Ethenyl-1H-indole

https://huagongshe.com/reaction/351576

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TributylvinyltinHCID 81998—
反応物Lithium ChlorideHCID 433294—
反応物7-BromoindoleHCID 2757020—
触媒TriphenylphosphineHCID 11776—
触媒HCID 178479785HCID 178479785—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物7-Ethenyl-1H-indoleHCID 1456740480%

反応条件

温度100 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06743785B2
出典データセットuspto-grants-2004_06
ORD IDord-0cfbd83475514974a0e7c40b96b6fc3f
出典メモuspto-grants-2004_06