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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26540Generated: October 25, 2026

Ethylene Glycol → 1-[2,2-Ethylenedioxy-2-(2-naphthyl)ethyl]imidazole

https://huagongshe.com/reaction/26540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium CarbonateHCID 11430—
ReactantNafimidone monohydrochlorideHCID 51199—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product1-[2,2-Ethylenedioxy-2-(2-naphthyl)ethyl]imidazoleHCID 3054123—

Reaction Steps

A mixture of 5.45 g. of 1-(2-naphthoylmethyl)imidazole hydrochloride, 2.49 g. ethylene glycol and 7.6 g. p-toluenesulfonic acid monohydrate in 50 ml. of toluene is heated overnight under reflux through a Dean-Stark trap. The trap is then replaced by a separatory funnel containing 4 A molecular seives and heating is continued for a further day. After cooling, the mixture is treated with 200 ml. of ethyl acetate, neutralized by pouring into excess aqueous potassium carbonate and the organic phase separated and dried (MgSO4) to afford a solution of 1-[2,2-ethylenedioxy-2-(2-naphthyl)ethyl]imidazole. The hydrochloride salt is prepared by dropwise addition of ethereal hydrogen chloride until precipitation is complete. Filtration and recrystallization from acetone/methanol gives 3.9 g. pure hydrochloride. m.p. 269°-270° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150153
Source datasetuspto-grants-1979_04
ORD IDord-f5f7466ae81b4ad3bd899d47583d00e1
Source noteuspto-grants-1979_04