Potassium hexafluorophosphate → HCID 86748381, compound
Reaction equation
[Cl-].[CH2:2]1[O:21][CH:5]([CH:6]2[CH:11]=[CH:10][CH:9]=[CH:8][N:7]2[CH2:12][C:13]2[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=2)[O:4][CH2:3]1.[F:22][P-:23]([F:28])([F:27])([F:26])([F:25])[F:24].[K+]>O>[F:22][P-:23]([F:28])([F:27])([F:26])([F:25])[F:24].[CH2:3]1[O:4][CH:5]([CH:6]2[CH:11]=[CH:10][CH:9]=[CH:8][N:7]2[CH2:12][C:13]2[CH:14]=[CH:15][C:16]([O:19][CH3:20])=[CH:17][CH:18]=2)[O:21][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1-(p-methoxybenzyl)pyridine-2-carboxaldehyde ethylene acetal chloride (10.0 g) was dissolved in water (100 mL) and was treated with potassium hexafluorophosphate (10.0 g). The precipitate which formed was collected by filtration and dried at 60° C. in vacuo to afford 9 g of 1-(p-methoxybenzyl)pyridine-2-carboxaldehyde ethylene acetal hexafluorophosphate (Formula X: R1 =R7 =H; R2 =4'--OCH3 ; X- =PF6-).
Workup
- customThe precipitate which formed
- filtrationwas collected by filtration
- customdried at 60° C. in vacuo
Sources & evidence
- ORD record
- ord-724decd9d8b64c259ca69f44c96966b1
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05380729
Reaction notes
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