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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232335생성일: 2026년 10월 26일

Tetrahydrofuran → 4-(1H-Imidazol-1-yl)phenyl-4-methyl-1-piperidine ethanol

https://huagongshe.com/reaction/232335

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물4-MethylpiperidineHCID 69381—
반응물alpha-(Bromomethyl)-4-(1H-imidazol-1-yl)benzenemethanolHCID 20031362—
생성물4-(1H-Imidazol-1-yl)phenyl-4-methyl-1-piperidine ethanolHCID 17845520—

반응 단계

Add α-(bromomethyl)-4-(1H-imidazol-1-yl)benzenemethanol (8.88 g, 33.24 mmol) to a room temperature solution of 4-methylpiperidine (11.8 mL, 99.73 mmol) in tetrahydrofuran (90mL). Stir the resultant mixture for 2.5 days and concentrate in vacuo. Chromatograph the residue on alumina (neutral, activity III, 100 g) using first methylene chloride than 2% methanol in methylene chloride as eluent. Collect the product fraction and concentrate in vacuo to give a solid. Recrystallize the solid from petroleum ether/ethyl acetate (ca. 4+1). Drying at 50° C. for 2 hr at p=1.0 mm affords the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04851526
출처 데이터셋uspto-grants-1989_07
ORD IDord-5c272afe37204cc6941c112a84e35e56
출처 메모uspto-grants-1989_07