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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1633131생성일: 2026년 10월 26일

Sodium hydride → 1-(8-Hydroxyoctyl)-2-(3-pyridyl)-3-methylindole

https://huagongshe.com/reaction/1633131

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2H-Pyran, 2-[(8-bromooctyl)oxy]tetrahydro-HCID 170916—
반응물3-Methyl-2-(3-pyridyl)indoleHCID 15591368—
용매DimethylformamideHCID 6228—
생성물1-(8-Hydroxyoctyl)-2-(3-pyridyl)-3-methylindoleHCID 20441661—

반응 단계

To a suspension of 2.9 g (0.06 mole) of 50% sodium hydride in mineral oil in 40 ml of dimethylformamide under nitrogen at 0°-5° is added dropwise over 20 minutes a solution of 10.4 g of 3-methyl-2-(3-pyridyl)indole in 60 ml of dimethylformamide. The mixture is stirred for 0.5 hour at 0°-5° followed by the dropwise addition of 17.6 g (0.06 mole) of 1-tetrahydropyranyloxy-8-bromooctane in 50 ml of dimethylformamide. After stirring at 0°-10° for 1 hour and at room temperature for 0.5 hour, the reaction mixture is poured into ice-water and extracted with ether. The ether extract is washed with water, dried over MgSO4 and evaporated to dryness. The residue is dissolved in 100 ml of 3N hydrochloric acid, the resulting mixture is kept at room temperature for 0.5 hour, washed with ether, basified with aqueous with 3N sodium hydroxide solution and extracted with methylene chloride. The methylene chloride solution is evaporated to dryness to give 1-(8-hydroxyoctyl)-2-(3-pyridyl)-3-methylindole.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04478842
출처 데이터셋uspto-grants-1984_10
ORD IDord-486f99ae28c54cac87d1b923e76288b0
출처 메모uspto-grants-1984_10