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HRID 11037作成日:2026年10月24日

Sodium hydride → 1-(3-{[Tert-butyl(dimethyl)silyl]oxy}propyl)-2-[2-(2-chlorophenyl)ethenyl]-5-methoxy-1h-indole

https://huagongshe.com/ja/reaction/11037

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物(3-Bromopropoxy)(tert-butyl)dimethylsilaneHCID 607486—
反応物2-[2-(2-Chlorophenyl)ethenyl]-5-methoxy-1H-indoleHCID 69583801—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-(3-{[Tert-butyl(dimethyl)silyl]oxy}propyl)-2-[2-(2-chlorophenyl)ethenyl]-5-methoxy-1h-indoleHCID 69583812—

反応手順

Sodium hydride (1.05 g of a 50% dispersion in mineral oil, 0.022 mol) was added to a solution of the 2-[2-(2-Chlorophenyl)ethenyl]-5-methoxy-1H-indole prepared according to example 37 (4.13 g, 0.014 mol) in DMF (30 mL) and the solution was stirred at room temperature for 5 min. 3-Bromopropyl tert-butyl(dimethyl)silyl ether (4.04 g, 0.016 mol) was added and stirring was continued for 2 h. The solution was diluted with water, extracted with EtOAc which was washed well with brine and the organic phase was dried, the drying agent was removed and the solution was concentrated to dryness to give 1-(3-{[tert-Butyl(dimethyl)silyl]oxy}propyl)-2-[2-(2-chlorophenyl)ethenyl]-5-methoxy-1H-indole (28) as an oily solid (4.98 g) (as a mixture of E/Z isomers) which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094798B1
出典データセットuspto-grants-2006_08
ORD IDord-4c6ae40223f9402a82a15bbacc3512f7
出典メモuspto-grants-2006_08