Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Lithium bis((trifluoromethyl)sulfonyl)azanide | HCID 3816071 | — |
| Reactant | HCID 178462722 | HCID 178462722 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178462731 | HCID 178462731 | 87% |
Reaction Steps
Yellow 1-ethyl-3-methylimidazolium chloride (Aldrich) (50 g) was dissolved in deionized water (250 mL). Decolorizing charcoal (3 g) was added to the solution and the resulting mixture heated at 65° C. for 24 hours. The solution was cooled to room temperature and filtered. To the yellow filtrate was added decolorizing charcoal (3 g) and the solution was then heated for a further 24 hours at 65° C. The solution was allowed to cool to room temperature and then filtered to give a colorless solution. This solution was poured into a solution of lithium bis(trifluoromethanesulfonyl)amide (115 g) in 200 mL of deionized water. The solution was then stirred at room temperature for 3 hrs after which two layers had formed. The bottom layer was separated and washed three times with deionized water (100 mL). The layer was then heated at 65° C. under vacuum for 48 hrs and then filtered through activated alumina to give 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide as a colorless clean dry material in 87% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763186B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-d791c06bcbb740e2be499f2c45814870 |
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| Source note | uspto-grants-2010_07 |
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