Reacción #8644

Ecuación de reacción

hexabromospirobifluorene

biphenylboronic acid

→

2,2′,4,4′,7,7′-hexabiphenylyl-9,9′-spirobifluorene

Disolventes

toluene

toluene

potassium carbonate

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroIn a 250 ml two-necked flask fitted
2. 2
   Temperaturawith reflux condenser and precision glass stirrer
3. 3
   TemperaturaThe mixture is refluxed under nitrogen
4. 4
   Temperaturaunder reflux for 7 hours
5. 5
   Filtraciónthe cooled solution is filtered
6. 6
   Extracciónthe filtrate is extracted twice
7. 7
   workup.STIRRINGby shaking with water (
8. 8
   Otrothe phase separation, chloroform
9. 9
   workup.ADDITIONis added)
10. 10
    SecadoThe organic phase is dried over sodium sulfate
11. 11
    Filtraciónfiltered through a short column of silica gel
12. 12
    Otrosubsequently evaporated on a rotary evaporator
13. 13
    OtroThe product is further purified by recrystallization from dichloromethane/pentane

Procedimiento

In a 250 ml two-necked flask fitted with reflux condenser and precision glass stirrer, 1.6 g of hexabromospirobifluorene and 3 g of biphenylboronic acid are slurried in a mixture of 50 ml of toluene and 50 ml of 1 M potassium carbonate solution. The mixture is refluxed under nitrogen and 115 mg of tetrakis(triphenylphosphine)palladium in 5 ml of toluene are added. The mixture is boiled under reflux for 7 hours while stirring. After the reaction is complete, the cooled solution is filtered and the filtrate is extracted twice by shaking with water (to improve the phase separation, chloroform is added). The organic phase is dried over sodium sulfate, filtered through a short column of silica gel and subsequently evaporated on a rotary evaporator. The product is further purified by recrystallization from dichloromethane/pentane. This gives 2 g (80%) of colorless crystals which fluoresce blue under UV illumination.

Fuente