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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1719389생성일: 2026년 10월 27일

Sodium hydride → 1-(7-Ethoxycarbonylheptyl)-2-(1-imidazolyl)-3-methylindole

https://huagongshe.com/reaction/1719389

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ethyl 8-bromooctanoateHCID 264813—
반응물2-(1-Imidazolyl)-3-methylindoleHCID 13280839—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물1-(7-Ethoxycarbonylheptyl)-2-(1-imidazolyl)-3-methylindoleHCID 20268191—

반응 단계

3-Methyl-2-(1-imidazolyl)indole (0.78 g) in dimethylformamide (8 ml) is added dropwise to a suspension of sodium hydride (50% dispersion in mineral oil, 0.20 g) in dimethylformamide (8 ml) stirred under nitrogen at 5°-10°. The resulting solution is stirred at 5°-10° for 1/2 hour. A solution of ethyl 8-bromooctanoate (1.00 g) in dimethylformamide (5 ml) is added dropwise. The reaction mixture is stirred at 5°-10° for 1/2 hour and then overnight at room temperature. The mixture is diluted with water (50 ml) and extracted into methylene chloride (3×25 ml). The extract is washed with water and saturated aqueous sodium chloride solution, dried over MgSO4, filtered, and concentrated in vacuo to give a two-phase oil. This oil is dissolved in ether (50 ml) and the solution is washed with water (5×25 ml) to remove dimethylformamide. The ether layer is dried over MgSO4, filtered, and concentrated in vacuo to give 1-(7-ethoxycarbonylheptyl)-2-(1-imidazolyl)-3-methylindole a viscous oil; NMR (CDCl3): δ 4.12 (q, 2H), 3.82 (t, 2H), 2.20 (s, 3H), 1.23 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04539410
출처 데이터셋uspto-grants-1985_09
ORD IDord-be37bbef19ba45daad1fdde8f7dd09ba
출처 메모uspto-grants-1985_09