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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1383962생성일: 2026년 10월 27일

Water → 1-[3-(Ethoxycarbonyl)-4-phenylbutyl]-2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazole

https://huagongshe.com/reaction/1383962

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 2-benzyl-4-bromobutanoateHCID 21188482—
반응물HCID 178423973HCID 178423973—
용매DimethylformamideHCID 6228—
생성물1-[3-(Ethoxycarbonyl)-4-phenylbutyl]-2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazoleHCID 21188596117.8%

반응 단계

A sodium hydride solution (60% in oil, 810 mg, 20.3 mmol) was washed with hexanes (2×50 ml) and then diluted with N,N-dimethylformamide (100 ml). At room temperature, under a nitrogen atmosphere, 2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazole (5.0 g, 18.3 mmol) was then added in one portion. The resulting mixture was then stirred at room temperature for thirty minutes, and then 3-(ethoxycarbonyl)-4-phenylbutyl bromide (5.79 g, 20.3 mmol) in N,N-dimethylformamide (10 ml) was added dropwise. Upon completion of this addition, the reaction mixture was stirred for about six hours at a temperature of 70-80° C. The reaction mixture was then cooled to room temperature, poured into water (500 ml), and then extracted with ethyl acetate (500 ml). The organic fraction was washed once with water (500 ml) and then dried over potassium carbonate. The solvents were removed in vacuo, yielding 10.28 grams of a dark oil. The crude material was further purified by flash silica gel chromatography, eluting with a gradient solvent of methylene chloride to 9:1 methylene chloride:ethyl acetate. The fractions containing the desired title product were combined and concentrated in vacuo to yield 8.08 grams (93%) of a viscous yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06255494B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-cf1eeb2e26c04411ac59ca0c904c6338
출처 메모uspto-grants-2001_07