Potassium 1,1,2,2-tetrafluoroethanesulfonate → HCID 178443227, compound

HRID 1019437Notes

Reaction equation

HRID 1019437 reaction equation
[Cl-].[CH2:2]([N+:14]1[CH:18]=[CH:17][N:16]([CH3:19])[CH:15]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13].[F:20][C:21]([F:29])([S:25]([O-:28])(=[O:27])=[O:26])[CH:22]([F:24])[F:23].[K+]>CC(C)=O>[F:20][C:21]([F:29])([S:25]([O-:28])(=[O:27])=[O:26])[CH:22]([F:24])[F:23].[CH2:2]([N+:14]1[CH:18]=[CH:17][N:16]([CH3:19])[CH:15]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]

Participants

4

Reactant 2

HCID 58905542Potassium 1,1,2,2-tetrafluoroethanesulfonateHCID 178443226HCID 178443226, compound2×

Product 1

HCID 178443227HCID 178443227, compound

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent2×

Conditions

Temperature
60 °C

Procedure

1-Dodecyl-3-methylimidazolium chloride (34.16 g, 0.119 moles) was partially dissolved in reagent-grade acetone (400 ml) in a large round-bottomed flask and stirred vigorously. Potassium 1,1,2,2-tetrafluoroethanesulfonate (TFES-K, 26.24 g, 0.119 moles) was added to reagent grade acetone (400 ml) in a separate round-bottomed flask, and this solution was carefully added to the 1-dodecyl-3-methylimidazolium chloride solution. The reaction mixture was heated at 60 degrees C. under reflux for approximately 16 hours. The reaction mixture was then filtered using a large frit glass funnel to remove the white KCl precipitate formed, and the filtrate was placed on a rotary evaporator for 4 hours to remove the acetone.

Workup

  1. temperatureunder reflux for approximately 16 hours
  2. filtrationThe reaction mixture was then filtered
  3. customto remove the white KCl precipitate
  4. customformed
  5. customthe filtrate was placed on a rotary evaporator for 4 hours
  6. customto remove the acetone

Sources & evidence

ORD record
ord-e0d71fd1041f48b6a39c06a5c8026bec
Source dataset
uspto-grants-2014_05
Patent number
US08715521B2

Reaction notes

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