Hydrochloric Acid → HCID 86636112, compound
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]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
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
- additionwas added
- customwas carried out at room temperature
- custom(20° C.)
- customfor 2 hours
- customreaction product
- customthe solvent was removed under reduced pressure
Sources & evidence
- ORD record
- ord-980e777b0d444d37a1be3a7a8a3263da
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08309740B2
Reaction notes
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