Réaction #66032
ord-ea826ef5f5ee438782a80e86607ef50a
Équation de réaction
Solvants
Conditions de réaction
Traitement
- 1Températureunder reflux
- 2AutreAfter completion of the reaction
- 3Extractionextracted with ethyl acetate (300 mL) and water (1000 mL)
- 4SéchageThe organic layer was dried with magnesium sulfate
- 5Concentrationconcentrated under reduced pressure
- 6Autreto obtain a solid
- 7Filtrationfiltered
- 8AutreThe filtrate was recrystallized in methanol (800 mL)
- 9FiltrationThe resultant solid was filtered
- 10Lavagewashed with hexane (300 mL)
Mode opératoire
1-Bromo-4-methoxynaphthalene (25 g, 0.105 mol), 4-(naphthalen-1-yl)phenylboronic acid (30.4 g, 0.137 mol), potassium carbonate (21.9 g, 0.16 mol), tetrakis(triphenylphosphine)palladium(0) (2.4 g, 0.01 mol), water (25 mL), tetrahydrofuran (75 mL) and toluene (75 mL) were stirred in a 250 mL round-bottom flask for 12 hours under reflux. After completion of the reaction, the reaction mixture was cooled to room temperature and extracted with ethyl acetate (300 mL) and water (1000 mL). The organic layer was dried with magnesium sulfate and concentrated under reduced pressure to obtain a solid. The solid was dissolved in hot toluene (400 mL) and then filtered. The filtrate was recrystallized in methanol (800 mL). The resultant solid was filtered and washed with hexane (300 mL) to obtain a product (20 g, 0.055 mol, 52.6%).