HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Bromobutyl)-4-methoxybenzene → 1-Heptyl-3-[4-(4-methoxyphenyl)butyl]-2,4,5-trimethylimidazolium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Bromobutyl)-4-methoxybenzene | HCID 578191 | — |
| Reactant | 1-Heptyl-2,4,5-trimethyl-1H-imidazole | HCID 20188300 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Heptyl-3-[4-(4-methoxyphenyl)butyl]-2,4,5-trimethylimidazolium bromide | HCID 23182139 | — |
Reaction Conditions
| Temperature | 125 °C |
|---|
Reaction Steps
Add 3.23 g (0.0133 mole) of 1-(4-bromobutyl)-4-methoxybenzene to 2.77 g (0.0133 mole) of 1-heptyl-2,4,5-trimethyl-1H-imidazole and heat at 125° C. for two hours. Follow the progress of the reaction by thin-layer chromatography on silica gel (methanol: 1M sodium chloride, 95:5). At the completion of the reaction, the cooled reaction mixture in 100 ml water and then wash with 100 ml cyclohexane. Extract aqueous layer with 150 ml methylenechloride and evaporate to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04613609 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-4dad2ecd3166437081e09be48b3902bb |
| Source note | uspto-grants-1986_09 |