HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylimidazole → Imidazolium cation
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | 3-(2-Bromoethoxy)-4-methylthiophene | HCID 22016338 | — |
| Product | Imidazolium cation | HCID 444234 | — |
| Product | 3-(2-Bromoethoxy)-4-methylthiophene | HCID 22016338 | — |
Reaction Steps
Similarly, monomer 2 is prepared from 3-(2-bromoethoxy)-4-methylthiophene (compound 4) and 1-methylimidazole (Aldrich Co.) (see Scheme 2). Compound 4 is prepared according to the procedure developed by Leclerc et al. (Faïd, K.; Leclerc, M. J. Chem. Soc., Chem. Commun., 2761, (1996)). The quaternization reaction between 1-methylimidazole and compound 4, provides the desired monomer imidazolium salt 2. (Lucas, P.; Mehdi, N. E.; Ho, H. A.; Belanger, D.; Breau, L. Synthesis, 9, 1253, (2000)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601503B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-7581edba7b174fef9d83ff4a785cbdcb |
| Source note | uspto-grants-2009_10 |