Reacción #976983

Ecuación de reacción

2,4-dimethylphenylamine

tert-butoxysodium

xylene

→

N4,N4′-bis(2,4-dimethylphenyl)-N4-p-tolylbiphenyl-4,4′-diamine

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroInto a 1 liter three-necked reaction vessel fitted with a cooling tube and a mechanical stirrer
2. 2
   Temperaturareflux for 5 hours in a nitrogen gas atmosphere
3. 3
   Temperaturawith heating in an oil bath
4. 4
   workup.WAITthe reaction mixture was left
5. 5
   Extracciónfollowed by extraction with toluene/water
6. 6
   Lavadowashing with hydrochloric acid water
7. 7
   workup.DISTILLATIONdistillation of the organic layer
8. 8
   Otrounder reduced pressure and purification with a silica gel column (developer solvent: hexane/toluene=1:1)

Procedimiento

Into a 1 liter three-necked reaction vessel fitted with a cooling tube and a mechanical stirrer, 88.5 g (0.2 mol) of (4′-(bromobiphenyl-4-yl)-(2,4-dimethylphenyl)-p-tolylamine, 26.7 g (0.22 mol) of 2,4-dimethylphenylamine, 2.2 g (0.01 mol) of palladium acetate, 11.1 g (0.02 mol) of bis(diphenylphosphino)ferrocene, 26.8 g (0.28 mol) of tert-butoxysodium and 400 mL of xylene were introduced to effect reflux for 5 hours in a nitrogen gas atmosphere and with heating in an oil bath. After the reaction was completed, the reaction mixture was left to cool to room temperature, followed by extraction with toluene/water, then washing with hydrochloric acid water, and thereafter distillation of the organic layer under reduced pressure and purification with a silica gel column (developer solvent: hexane/toluene=1:1) to give the desired N4,N4′-bis(2,4-dimethylphenyl)-N4-p-tolylbiphenyl-4,4′-diamine. The compound obtained was in a yield of 71.4 g corresponding to 74%. The compound obtained was measured with the same elementary analyzer as the above.

Fuente