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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26538Generated: October 25, 2026

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

https://huagongshe.com/reaction/26538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
Reactant2-Bromo-2'-acetonaphthoneHCID 69179—
SolventWaterHCID 962—
Product2-(1H-Imidazol-1-yl)-1-(2-naphthalenyl)ethanoneHCID 51200—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150153
Source datasetuspto-grants-1979_04
ORD IDord-3d04a86e7ddd4200adbb26a4d36e667b
Source noteuspto-grants-1979_04