HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296812Generated: October 25, 2026
1-Methylimidazole → 1-Ethyl-3-methylimidazolium trifluoromethanesulfonate
https://huagongshe.com/reaction/1296812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | Ethyl trifluoromethanesulphonate | HCID 67924 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1-Ethyl-3-methylimidazolium trifluoromethanesulfonate | HCID 2758874 | 99.1% |
Reaction Steps
6.31 g (0.0768 mol) of 1-methylimidazole in 50 ml of dry hexane are introduced into a round-bottomed flask fitted with a reflux condenser. 13.75 g (0.0772 mol) of ethyl triflate are added over the course of 20 minutes with constant stirring and cooling with the aid of an ice bath. After a further 10 minutes, the ice bath is then replaced by an oil bath, and the reaction mixture is refluxed for one hour (oil-bath temperature 70-75° C.). After the hexane has been removed by distillation, the reaction mixture which remains is held at 80-90° C. in a 30-100 Pa vacuum for 5 hours, giving 19.80 g (yield: 99.1%) of 1-methyl-3-ethylimidazolium trifluoromethanesulfonate as a transparent, colourless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07247740B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-befd09c930ef40a8842be91fc4614881 |
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| Source note | uspto-grants-2007_07 |
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