Potassium hexafluorophosphate → HCID 178443029, compound

HRID 1943312Notes

Reaction equation

HRID 1943312 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

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

  1. filtrationThe precipitate is filtered
  2. washwashed 3 times with 30 mL
  3. distillationdistilled water
  4. 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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