HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dimethylimidazole → 1,2-Dimethyl-3-propylimidazolium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dimethylimidazole | HCID 15617 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,2-Dimethyl-3-propylimidazolium iodide | HCID 11459786 | 92% |
Reaction Steps
1,2-dimethylimidazole (7.2 g, made by Aldrich) and propyl iodide (12.7 g, made by Kanto Chemical) were stirred in toluene at 75° C. for 15 hours. After the end of the reaction, the reaction mixture was cooled to room temperature and the crude crystals formed were recovered. A mixed solvent of toluene and isopropanol was used for recrystallization. The crystals were dried in vacuo to obtain 1,2-dimethyl-3-propylimidazolium iodide (18.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481849B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-4ebc76d7580e4d18916bcf4bab2576f9 |
| Source note | uspto-grants-2013_07 |