HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019435Generated: October 25, 2026
Potassium Chloride → HCID 178462732, compound
https://huagongshe.com/reaction/1019435
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Chloride | HCID 4873 | — |
| Reactant | Potassium 1,1,2,2-tetrafluoroethanesulfonate | HCID 58905542 | — |
| Reactant | HCID 178462722 | HCID 178462722 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178462732 | HCID 178462732 | 64% |
Reaction Steps
To a 500 ml round bottom flask was added 1-ethyl-3methylimidazolium chloride (Emim-Cl, 98%, 61.0 g) and reagent grade acetone (500 ml). The mixture was gently warmed (50 degrees C.) until almost all of the Emim-Cl dissolved. To a separate 500 ml flask was added potassium 1,1,2,2-tetrafluoroethanesulfonate (TFES-K, 90.2 g) along with reagent grade acetone (350 ml). This second mixture was stirred magnetically at 24 degrees C. until all of the TFES-K dissolved. These solutions were combined in a 1 l flask producing a milky white suspension. The mixture was stirred at 24 degrees C. for 24 hrs. The KCl precipitate was then allowed to settle leaving a clear green solution above it. The reaction mixture was filtered once through a celite/acetone pad and again through a fritted glass funnel to remove the KCl. The acetone was removed in vacuo first on a rotovap and then on a high vacuum line (4 Pa, 25 degrees C.) for 2 hr. The product was a viscous light yellow oil (76.0 g, 64% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08715521B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-59adb1bea6894374bb1d576fc785a7bb |
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| Source note | uspto-grants-2014_05 |
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