Reaktion #68714

Reaktionsgleichung

potassium carbonate

4-bromodiphenylamine

9-phenyl-9H-carbazole-3-boronic acid

tri(o-tolyl)phosphine

→

white solid

Ausbeute 45.9%

4-(9-phenyl-9H-carbazol-3-yl)diphenylamine

Ausbeute 45.9%

Lösungsmittel

ethanol

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeInto a 500 mL three-neck flask were put
2. 2
   SonstigeUnder reduced pressure, this mixture was degassed
3. 3
   SonstigeAfter the reflux, the organic layer of the mixture was separated
4. 4
   Extraktionthe aqueous layer was extracted with toluene
5. 5
   Waschenwashed with a saturated aqueous sodium chloride solution
6. 6
   TrocknenThe combined organic layer was dried with magnesium sulfate
7. 7
   FiltrationAfter the drying, this mixture was subjected to gravity filtration
8. 8
   Sonstigecondensed
9. 9
   Sonstigeto give an oily light brown substance
10. 10
    SonstigeThis oily substance was purified by silica gel column chromatography (a developing solvent
11. 11
    SonstigeAfter the purification
12. 12
    Sonstigecondensed
13. 13
    Sonstigeto give a white solid
14. 14
    SonstigeThe white solid was recrystallized with a mixed solvent of dichloromethane and hexane

Vorschrift

Into a 500 mL three-neck flask were put 6.5 g (26 mmol) of 4-bromodiphenylamine, 7.5 g (26 mmol) of 9-phenyl-9H-carbazole-3-boronic acid, and 400 mg (1.3 inmol) of tri(o-tolyl)phosphine. The air in the flask was replaced with nitrogen. To the mixture were added 100 mL of toluene, 50 mL of ethanol, and 14 mL of an aqueous solution of potassium carbonate (0.2 mol/L). Under reduced pressure, this mixture was degassed while being stirred. After the degassing, 67 mg (30 mmol) of palladium(II) acetate was added to the mixture. This mixture was refluxed at 100° C. for 10 hours. After the reflux, the organic layer of the mixture was separated, the aqueous layer was extracted with toluene, and the extracted solution was combined with the organic layer and then washed with a saturated aqueous sodium chloride solution. The combined organic layer was dried with magnesium sulfate. After the drying, this mixture was subjected to gravity filtration. The obtained filtrate was condensed to give an oily light brown substance. This oily substance was purified by silica gel column chromatography (a developing solvent was a mixed solvent of hexane:toluene=4:6). After the purification, the substance was condensed to give a white solid. The white solid was recrystallized with a mixed solvent of dichloromethane and hexane to give 4.9 g of a white solid, which was the object of the synthesis, in a yield of 45%. A synthesis scheme of Step 2 is shown in (a-2) given below.

Quelle