HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 4-[2-(4-Propylphenoxy)ethyl]-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Propylphenol | HCID 12580 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(2-chloroethyl)-1H-imidazole hydrochloride | HCID 178478570 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[2-(4-Propylphenoxy)ethyl]-1H-imidazole | HCID 178439271 | — |
Reaction Steps
240 mg (60% in oil; 6 mmol) of sodium hydride are slowly added to a solution of 1.63 g (12 mmol) of 4-propylphenol in 10 ml of dimethylformamide and the mixture is stirred at room temperature for 1 hour. 200 mg (1.2 mmol) of 4-(2-chloroethyl)-1H-imidazole hydrochloride and tetrabutylammonium iodide are added and the mixture is stirred at 80° C. for 3 days. The reaction mixture is cooled and 150 ml of diethyl ether are added. The precipitate is separated by filtration and the filtrate is evaporated under reduced pressure to give a residue which is purified by preparative high performance chromatography. The title compound is converted to the oxalate (from an ethanol/diethyl ether mixture), M.p.: 168°-171° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05708171 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-e2d344935a8e4b058f1d5b877e6be2c7 |
| Source note | uspto-grants-1998_01 |