Réaction #992721
ord-eb18b4e62a04466488466fc2a5dbf418
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1TempératureThe mixture was heated up to 135° C.
- 2Températureheated at this temperature
- 3workup.STIRRINGwith stirring for 4 hours
- 4TempératureThe reaction mixture was cooled to room temperature
- 5AutreThe organic layer was separated from the aqueous layer
- 6Lavagethe aqueous layer was washed with 200 ml of toluene
- 7Concentrationconcentrated
- 8Autredried under reduced pressure
- 9Autreto give 9.5 g of a crude product
- 10Autredried under reduced pressure
Mode opératoire
To a solution of 0.161 g (0.715 millimole) of palladium (II) acetate in 20 ml of xylene was added 0.58 g (2.86 millimoles) of tri-tert-butylphosphine and the mixture was heated at 80° C. for 30 minutes with stirring. This solution was transferred into a solution heated at 80° C. of 5.24 g (0.0143 mole) of 2,7-bis(phenylamino)dibenzodioxin, 7.41 g (0.0358 mole) of 1-bromonaphthalene, and 5.77 g (0.06 mole) of sodium tert-butoxide in 260 ml of xylene. The mixture was heated up to 135° C. and heated at this temperature with stirring for 4 hours. The reaction mixture was cooled to room temperature, and 200 ml of water was added. The organic layer was separated from the aqueous layer, the aqueous layer was washed with 200 ml of toluene, and the organic layers were combined, concentrated, and dried under reduced pressure to give 9.5 g of a crude product. The crude product was subjected to reslurrying under heat with ethyl acetate and dried under reduced pressure to give 3.40 g (0.0055 mole, 38.5% yield) of 2,7-bis(N-1-naphthyl-N-phenylamino)dibenzodioxin. The product showed a purity of 98.3 area % (HPLC, 254 nm). The product was purified further by sublimation; FD-MS, m/z 618 [M]+, m.p. 315° C., Tg 103° C.