Reaction #2316915
ord-ee8f535af90c441e8d6bf5517e70e291
Reaction equation
triphenylcyclopropenylium chloride
sodium hexafluoroantimonate
triphenylcyclopropenylium chloride
→
Triphenylcyclopropenylium hexafluoroantimonate
Reactants
Reagents
None
Solvents
Conditions
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1OtherNaCl was removed by filtration
- 2Washwashed with CH3CN
- 3workup.ADDITIONTo the filtrate was added ether
- 4FiltrationAfter filtration
- 5Othera white, very light yellow solid was obtained
- 6Otherwas between about 319 and 321° C.
Procedure
Triphenylcyclopropenylium hexafluoroantimonate was synthesized by the metatheses of triphenylcyclopropenylium chloride with sodium hexafluoroantimonate in acetonitrile. 0.003 moles of the triphenylcyclopropenylium chloride (literature) of Example 1 and 0.0031 moles of SbF6 was each separately dissolved in 10 ml of CH3CN and then combined. NaCl was removed by filtration and washed with CH3CN. To the filtrate was added ether. After filtration, a white, very light yellow solid was obtained. The melting point of this solid was between about 319 and 321° C.