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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11037생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물(3-Bromopropoxy)(tert-butyl)dimethylsilaneHCID 607486—
반응물2-[2-(2-Chlorophenyl)ethenyl]-5-methoxy-1H-indoleHCID 69583801—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-(3-{[Tert-butyl(dimethyl)silyl]oxy}propyl)-2-[2-(2-chlorophenyl)ethenyl]-5-methoxy-1h-indoleHCID 69583812—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094798B1
출처 데이터셋uspto-grants-2006_08
ORD IDord-4c6ae40223f9402a82a15bbacc3512f7
출처 메모uspto-grants-2006_08