Reaktion #219690

Reaktionsgleichung

sodium tert-butoxide

tri-tert-butylphosphine

N-(9-anthracenyl)-N-phenylamine

4,4′-dibromo-2,2′,3,3′,5,5′,6,6′-octafluoro-1,1′-biphenyl

→

4-bromo-4′-[N-(9-anthracenyl)-N-phenylamino]-2,2′,3,3′,5,5′,6,6′-octafluoro-1,1′-biphenyl

Ausbeute 67.2%

Lösungsmittel

toluene

water

toluene

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwas dropped into the mixture and it
2. 2
   workup.STIRRINGwas stirred for 30 minutes
3. 3
   workup.ADDITIONwas then dropped
4. 4
   TemperaturThen, the mixture was heated
5. 5
   workup.STIRRINGstirred for about 8 hours in an oil bath
6. 6
   Temperaturheated at 120° C
7. 7
   Sonstigeto room temperature
8. 8
   Sonstigethe resultant solution was then separated into an aqueous layer
9. 9
   ExtraktionFurthermore, the aqueous layer was extracted with toluene and ethyl acetate
10. 10
    Trocknendried with magnesium sulfate
11. 11
    SonstigeThe solvent was evaporated
12. 12
    Sonstigethe residue was purified by silicagel-column chromatography (toluene:hexane=1:2)

Vorschrift

In a nitrogen flow, 160 mg (0.282 mmol) of palladium bis(benzylideneacetone) and 170 mg (0.846 mmol) of tri-tert-butylphosphine were dissolved in 40 ml of toluene and then stirred for 15 minutes at room temperature. Then, 0.58 g (1.27 mmol) of 4,4′-dibromo-2,2′,3,3′,5,5′,6,6′-octafluoro-1,1′-biphenyl dissolved in 50 ml of toluene was dropped into the mixture and it was stirred for 30 minutes. Furthermore, 0.34 g (1.27 mmol) of N-(9-anthracenyl)-N-phenylamine was dissolved in 50 ml of toluene and was then dropped therein, followed by the addition of 0.18 g (1.91 mmol) of sodium tert-butoxide. Then, the mixture was heated and stirred for about 8 hours in an oil bath heated at 120° C. After returning the reaction solution to room temperature, 50 ml of water was added thereto and the resultant solution was then separated into an aqueous layer and an organic layer. Furthermore, the aqueous layer was extracted with toluene and ethyl acetate, and was then combined with the previous organic layer and dried with magnesium sulfate. The solvent was evaporated and then the residue was purified by silicagel-column chromatography (toluene:hexane=1:2) to obtain 0.55 g of 4-bromo-4′-[N-(9-anthracenyl)-N-phenylamino]-2,2′,3,3′,5,5′,6,6′-octafluoro-1,1′-biphenyl.

Quelle