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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Nafimidone monohydrochloride | HCID 51199 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-[2,2-Ethylenedioxy-2-(2-naphthyl)ethyl]imidazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04150153 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-f5f7466ae81b4ad3bd899d47583d00e1 |
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| Source note | uspto-grants-1979_04 |
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