Sodium hexafluorophosphate → HCID 18468789, compound

HRID 2229734Notes

Reaction equation

HRID 2229734 reaction equation
[Cl-].[C:2]1([C:8]2([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[C+:10]=[C:9]2[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[F:23][P-:24]([F:29])([F:28])([F:27])([F:26])[F:25].[Na+]>C(#N)C>[F:23][P-:24]([F:29])([F:28])([F:27])([F:26])[F:25].[C:17]1([C:8]2([C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[C+:10]=[C:9]2[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Participants

4

Reactant 2

HCID 5147921Sodium hexafluorophosphateHCID 18468792HCID 18468792, compound

Product 1

HCID 18468789HCID 18468789, compound

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

Triphenylcyclopropenylium hexafluorophosphate was synthesized through the metathesis of triphenylcyclopropenylium chloride with sodium hexafluorophosphate in acetonitrile. The resulting white crystalline compound had a melting point of 310° C.

Sources & evidence

ORD record
ord-ca11a36085984b2e96fd88fb594716b2
Source dataset
uspto-grants-2002_07
Patent number
US06420460B1

Reaction notes

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