Reaktion #1532479

Reaktionsgleichung

4-nitrodiphenylamine

sodium tert-butoxide

4,4′-dibromobiphenyl

tri-t-butylphosphine

→

N,N′-diphenyl-N,N′-bis(4-aminophenyl)-1,1-biphenyl-4,4′-diamine

Lösungsmittel

p-xylene

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigea reaction
2. 2
   Sonstigeat about 150° C.
3. 3
   Sonstigefor about 16 hours
4. 4
   Filtrationa resultant solution was filtered
5. 5
   Sonstigeto remove solid matter
6. 6
   workup.DISSOLUTIONdissolved in excess chloroform
7. 7
   FiltrationThe salt was filtered
8. 8
   workup.DISTILLATIONusing distilled water
9. 9
   Einengenthe resultant solution was then concentrated
10. 10
    SonstigeThen, purification
11. 11
    Sonstigewas performed through column chromatography and recrystallization
12. 12
    workup.DISSOLUTIONThe acquired powder was dissolved in 50 mL ethanol
13. 13
    workup.ADDITION1.5 mL hydrazine monohydrate was added
14. 14
    Temperaturby refluxing for 24 hours

Vorschrift

In a 100 mL three-necked flask were dissolved 1.56 g of 4,4′-dibromobiphenyl, 2.30 g of 4-nitrodiphenylamine, 1.44 g of sodium tert-butoxide and 0.51 g of tris(dibenzylideneacetone) dipalladium in 50 mL of p-xylene, followed by adding 0.3 mL of tri-t-butylphosphine to the resultant mixture, causing a reaction to take place under a nitrogen atmosphere at about 150° C. for about 16 hours. After the reaction was completed, a resultant solution was filtered to remove solid matter, and dissolved in excess chloroform. The salt was filtered using distilled water and the resultant solution was then concentrated. Then, purification was performed through column chromatography and recrystallization, acquiring 1.2 g of N,N′-diphenyl-N,N′-bis(4-nitrophenyl)-1,1-biphenyl-4,4′-diamine in the form of powder. The acquired powder was dissolved in 50 mL ethanol, 1.5 mL hydrazine monohydrate was added thereto with a catalytic amount of 10% Pd/C, followed by refluxing for 24 hours, yielding 0.9 g of N,N′-diphenyl-N,N′-bis(4-aminophenyl)-1,1-biphenyl-4,4′-diamine.

Quelle