Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | 2-Methylimidazole | HCID 12749 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 86654826 | HCID 86654826 | — |
Reaction Steps
2-Methylimidazole was allowed to react with one equivalent of sodium hydride at room temperature in 1,2-dimethoxyethane as a solvent, and then three equivalents of 1-bromopropane was slowly added thereto, followed by stirring at 60° C. for two days. About one day after the start of stirring, an adequate amount of 2-propanol was added thereto as a co-solvent. After the completion of stirring, the solvent and unreacted 1-bromopropane were distilled off. The residual solid was recrystallized twice from acetone to give 1,3-di-n-propyl-2-methylimidazolium bromide as transparent and colorless crystals (ionic liquid No. 3 in Table 1). Then, 1,3-di-n-propyl-2-methylimidazolium bromide was dissolved in water, and one equivalent of silver sulfate was added thereto, followed by stirring for about 1 hour at room temperature. The resultant precipitate of silver bromide was removed by filtration, and then water was distilled off. The residual solid was recrystallized from acetonitrile to give 1,3-di-n-propyl-2-methylimidazolium sulfate as white fine crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08449862B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-cb37c7cf4d4341259f1d38a120742dbc |
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| Source note | uspto-grants-2013_05 |
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