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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 232335Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/232335

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
Edukt4-MethylpiperidineHCID 69381—
Eduktalpha-(Bromomethyl)-4-(1H-imidazol-1-yl)benzenemethanolHCID 20031362—
Produkt4-(1H-Imidazol-1-yl)phenyl-4-methyl-1-piperidine ethanolHCID 17845520—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04851526
Quelldatensatzuspto-grants-1989_07
ORD IDord-5c272afe37204cc6941c112a84e35e56
Quellennotizuspto-grants-1989_07