Reacción #2072758

ord-7e3731b0f9c240b98630560fceae33ce

Ecuación de reacción

CCCCCCCCCCCC[n+]1ccn(C)c1.[Cl-]
1-Dodecyl-3-methylimidazolium chloride
O=S(=O)([O-])C(F)(F)C(F)F.[K+]
Potassium 1,1,2,2-tetrafluoroethanesulfonate
CCCCCCCCCCCC[n+]1ccn(C)c1.[Cl-]
1-dodecyl-3-methylimidazolium chloride
CCCCCCCCCCCC[n+]1ccn(C)c1.O=S(=O)([O-])C(F)(F)C(F)F
1-dodecyl-3-methylimidazolium 1,1,2,2-tetrafluoroethanesulfonate

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaunder reflux for approximately 16 hours
  2. 2
    FiltraciónThe reaction mixture was then filtered
  3. 3
    Otroto remove the white KCl precipitate
  4. 4
    Otroformed
  5. 5
    Otrothe filtrate was placed on a rotary evaporator for 4 hours
  6. 6
    Otroto remove the acetone

Procedimiento

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° 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07544813B2uspto-grants-2009_06