Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26538Erstellt: 24. Oktober 2026

Imidazole → 2-(1H-Imidazol-1-yl)-1-(2-naphthalenyl)ethanone

https://huagongshe.com/de/reaction/26538

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktDimethylformamideHCID 6228—
Edukt2-Bromo-2'-acetonaphthoneHCID 69179—
LösungsmittelWaterHCID 962—
Produkt2-(1H-Imidazol-1-yl)-1-(2-naphthalenyl)ethanoneHCID 51200—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred, ice-cooled slurry of 35 g. of imidazole in 25 ml. of dimethylformamide is added 24.9 g. of bromomethyl 2-naphthyl ketone. The mixture is stirred for 2 hours at 0° C., and then allowed to come to room temperature and stirred overnight. The solution is poured into water and the resulting sticky solid filtered off, washed with water and dissolved in benzene. Thereafter the resultant benzene solution is dried (azeotroped) to afford 1-(2-naphthoylmethyl)imidazole which is converted to its hydrochloride acid addition salt by addition of ethereal hydrogen chloride until precipitation is complete. The salt is crystallized by the addition of ethyl acetate and the resulting solid recrystallized from methanol/acetone to yield colorless needles of 1-(2-naphthoylmethyl)imidazole hydrochloride, m.p. 226°-228.5° C. (decomp.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04150153
Quelldatensatzuspto-grants-1979_04
ORD IDord-3d04a86e7ddd4200adbb26a4d36e667b
Quellennotizuspto-grants-1979_04