Hydrochloric Acid → HCID 86636112, compound

HRID 1877319Notes

Reaction equation

HRID 1877319 reaction equation
[CH3:1][N:2]1[CH:6]=[CH:5][N:4]=[CH:3]1.[ClH:7].[F:8][C:9]([F:16])=[C:10]([F:15])[C:11]([F:14])([F:13])[F:12]>C(#N)C>[Cl-:7].[CH3:1][N+:2]1[CH:6]=[CH:5][N:4]([C:9]([F:16])([F:8])[CH:10]([F:15])[C:11]([F:14])([F:13])[F:12])[CH:3]=1

Participants

5

Procedure

1-Methylimidazole (10 mmol) was dissolved in acetonitrile (20 mL) in a 100 mL high pressure reactor, and HCl (ether solution, 10 mmol) was added slowly. After sealing the reactor and removing air, 1,1,2,3,3,3-hexafluoropropylene (20 mmol) was added and stirring was carried out at room temperature (20° C.) for 2 hours. Pressure inside the reactor, which was initially maintained at room temperature at about 60 psig by 1,1,2,3,3,3-hexafluoropropylene, decreased as the reaction occurred. When the pressure did not decrease any more, reaction product was taken from the reactor and the solvent was removed under reduced pressure. The reaction product 1-methyl-3-(1,1,2,3,3,3-hexafluoropropyl)imidazolium chloride was obtained as white solid. Yield of the obtained ionic liquid was calculated by the following Equation 1.

Workup

  1. additionwas added
  2. customwas carried out at room temperature
  3. custom(20° C.)
  4. customfor 2 hours
  5. customreaction product
  6. customthe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-980e777b0d444d37a1be3a7a8a3263da
Source dataset
uspto-grants-2012_11
Patent number
US08309740B2

Reaction notes

Loading…