Potassium hexafluorophosphate → HCID 178443029, compound
Reaction equation
[Br-].[CH2:2]([N+:18]1[CH:22]=[CH:21][N:20]([CH2:23][C:24]2[CH:29]=[CH:28][C:27]([C:30]3[O:31][C:32]([C:35]4[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=4)=[CH:33][N:34]=3)=[CH:26][CH:25]=2)[CH:19]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].[F:41][P-:42]([F:47])([F:46])([F:45])([F:44])[F:43].[K+]>C(O)C>[F:41][P-:42]([F:47])([F:46])([F:45])([F:44])[F:43].[CH2:2]([N+:18]1[CH:22]=[CH:21][N:20]([CH2:23][C:24]2[CH:29]=[CH:28][C:27]([C:30]3[O:31][C:32]([C:35]4[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=4)=[CH:33][N:34]=3)=[CH:26][CH:25]=2)[CH:19]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a round-bottomed flask are added 1-hexadecyl-3-[4-(5-phenyl-oxazol-2-yl)-benzyl]-3H-imidazol-1-ium bromide (1.008 g, 1.7 mmol) dissolved in ethanol (50 mL). An aqueous solution of potassium hexafluorophosphate is added (0.490 g, 2.7 mmol, 10 mL). The mixture is stirred at ambient temperature for 3 days. The precipitate is filtered, washed 3 times with 30 mL distilled water and dried under reduced pressure at ambient temperature for 12 hours. The product is characterized by NMR spectroscopy.
Workup
- filtrationThe precipitate is filtered
- washwashed 3 times with 30 mL
- distillationdistilled water
- customdried under reduced pressure at ambient temperature for 12 hours
Sources & evidence
- ORD record
- ord-f4e6402a9cb84cfa91bf245b336ca7ce
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08389940B2
Reaction notes
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