Potassium Chloride → HCID 178462732, compound

HRID 1019435Notes

Reaction equation

HRID 1019435 reaction equation
[Cl-].[CH2:2]([N+:4]1[CH:8]=[CH:7][N:6]([CH3:9])[CH:5]=1)[CH3:3].[F:10][C:11]([F:19])([S:15]([O-:18])(=[O:17])=[O:16])[CH:12]([F:14])[F:13].[K+].[Cl-].[K+]>CC(C)=O>[F:10][C:11]([F:19])([S:15]([O-:18])(=[O:17])=[O:16])[CH:12]([F:14])[F:13].[CH2:2]([N+:4]1[CH:8]=[CH:7][N:6]([CH3:9])[CH:5]=1)[CH3:3]

Participants

5

Conditions

Temperature
24 °C

Procedure

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).

Workup

  1. dissolutiondissolved
  2. customThese solutions were combined in a 1 l flask
  3. customproducing a milky white suspension
  4. stirringThe mixture was stirred at 24 degrees C
  5. customto settle leaving a clear green solution above it
  6. filtrationThe reaction mixture was filtered once through a celite/acetone pad and again through a fritted glass funnel
  7. customto remove the KCl
  8. customThe acetone was removed in vacuo first on a rotovap
  9. waiton a high vacuum line (4 Pa, 25 degrees C.) for 2 hr

Sources & evidence

ORD record
ord-59adb1bea6894374bb1d576fc785a7bb
Source dataset
uspto-grants-2014_05
Patent number
US08715521B2

Reaction notes

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