تفاعل #1106620

ord-8bc3c33a57394ef0b2425325324163b6

معادلة التفاعل

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

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةunder reflux for approximately 16 hours
  2. 2
    ترشيحThe reaction mixture was then filtered
  3. 3
    أخرىto remove the white KCl precipitate
  4. 4
    أخرىformed
  5. 5
    أخرىthe filtrate was placed on a rotary evaporator for 4 hours
  6. 6
    أخرىto remove the acetone

الإجراء التجريبي

1-Hexadecyl-3-methylimidazolium chloride (17.0 g, 0.0496 moles) was partially dissolved in reagent-grade acetone (100 ml) in a large round-bottomed flask and stirred vigorously. Potassium 1,1,2,2-tetrafluoroethanesulfonate (TFES-K, 10.9 g, 0.0495 moles) was added to reagent grade acetone (100 ml) in a separate round-bottomed flask, and this solution was carefully added to the 1-hexadecyl-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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08715521B2uspto-grants-2014_05