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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498903Generated: October 25, 2026

Potassium Chloride → HCID 178448553, compound

https://huagongshe.com/reaction/498903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium ChlorideHCID 4873—
ReactantPotassium;1,1,2-trifluoro-2-(1,1,2,2,2-pentafluoroethoxy)ethanesulfonateHCID 87096009—
ReactantHCID 178448538HCID 178448538—
SolventAcetoneHCID 180—
ProductHCID 178448553HCID 17844855362%

Reaction Steps

1-Butyl-3-methylimidazolium chloride (Bmim-Cl, 7.8 g) and dry acetone (150 ml) were combined at room temperature in a 500 ml flask. At room temperature in a separate 200 ml flask, potassium 1,1,2-trifluoro-2-(perfluoroethoxy)ethanesulfonate (TPES-K, 15.0 g) was dissolved in dry acetone (300 ml). These two solutions were combined and allowed to stir magnetically for 12 hr under positive nitrogen pressure. The KCl precipitate was then allowed to settle leaving a colorless 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. Residual KCl was still precipitating out of the solution, so methylene chloride (50 ml) was added to the crude product, which was then washed with deionized water (2×50 ml). The solution was dried over magnesium sulfate, and the solvent was removed in vacuo to give the product as a viscous light yellow oil (12.0 g, 62% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07765823B2
Source datasetuspto-grants-2010_08
ORD IDord-bb154c89e28c4b1f8428b07c467ceca8
Source noteuspto-grants-2010_08