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HRID 910069作成日:2026年10月25日

Water → 7-Ethenyl-1H-indole

https://huagongshe.com/reaction/910069

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

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08022065B2
出典データセットuspto-grants-2011_09
ORD IDord-f956cce919854dba9fea3f949893433e
出典メモuspto-grants-2011_09