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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 374043생성일: 2026년 10월 25일

Ethyl 5-bromovalerate → 5-(4,5-diphenyl-1H-imidazol-2-ylthio)pentanoic acid ethyl ester

https://huagongshe.com/reaction/374043

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 5-bromovalerateHCID 84580—
반응물Sodium BicarbonateHCID 516892—
반응물HCID 178527825HCID 178527825—
용매DimethylformamideHCID 6228—
생성물5-(4,5-diphenyl-1H-imidazol-2-ylthio)pentanoic acid ethyl esterHCID 5420157968%

반응 단계

Part A. To a solution of 4,5-diphenyl-2-imidazolethiol (25.2 g, 0.1 mol) in N,N-dimethylformamide (250 mL) was added, dropwise, a solution of ethyl 5-bromopentanoate (23.73 mL, 31.35 g, 0.15 mol) in N,N-dimethylformamide (80 mL), and the reaction mixture was stirred at reflux under nitrogen for 18 hours. The reaction mixture was cooled, poured into 5% sodium bicarbonate and ice, and then extracted with ethyl acetate. The combined organic extracts were washed sequentially with 5% sodium bicarbonate, water, saturated sodium chloride solution, dried over magnesium sulfate, and concentrated under vacuum. The residue was chromatographed with 7:3 hexane-ethyl acetate, and the resulting solid was recrystallized from acetonitrile and triturated with hexane to give 5-(4,5-diphenyl-1H-imidazol-2-ylthio)pentanoic acid ethyl ester (25.95 g, 0.068 mol) as a white solid, mp 87°-89°. 1H NMR (DMSO-d6) δ7.55-7.15(m,11H), 4.0(q,2H,J=8Hz), 2.9(t,2H,J=7Hz), 2.3(t,2H,J=7Hz), 1.9-1.6(m,4H), 1.2(t,3H,J=8Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05166214
출처 데이터셋uspto-grants-1992_11
ORD IDord-94e02df17a0e4fa39f3ec2ef9694a5ca
출처 메모uspto-grants-1992_11