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HRID 232335作成日:2026年10月26日

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

https://huagongshe.com/reaction/232335

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物4-MethylpiperidineHCID 69381—
反応物alpha-(Bromomethyl)-4-(1H-imidazol-1-yl)benzenemethanolHCID 20031362—
生成物4-(1H-Imidazol-1-yl)phenyl-4-methyl-1-piperidine ethanolHCID 17845520—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04851526
出典データセットuspto-grants-1989_07
ORD IDord-5c272afe37204cc6941c112a84e35e56
出典メモuspto-grants-1989_07