Réaction #155317

Équation de réaction

7-bromo-5-methylbenzofuran

benzophenone imine

sodium t-butoxide

ammonium chloride

→

benzhydrylidene(5-methylbenzofuran-7-yl) amine

Rendement 125.0%

Solvants

water

Conditions de réaction

Traitement

1. 1
   Températurewhile heating
2. 2
   Températureunder reflux in a nitrogen atmosphere
3. 3
   Extractionfollowed by extraction
4. 4
   SéchageThe organic layer was dried over anhydrous magnesium sulfate
5. 5
   Concentrationconcentrated to dryness under reduced pressure
6. 6
   AutreThe residue was purified
7. 7
   AutreThe solvent was removed under a reduced pressure

Mode opératoire

To a 7-bromo-5-methylbenzofuran (9.71 g, 46 mmol) toluene solution (100 ml) were added a benzophenone imine (10.25 g, 56 mmol) toluene solution (55 ml), tris(dibenzylideneacetone)dipalladium (1.1 g, 1 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP, 2.1 g, 3.45 mmol), and sodium t-butoxide (3.1 g, 31 mmol). The resulting mixture was then stirred for 4 hours while heating under reflux in a nitrogen atmosphere. The reaction mixture was cooled to room temperature, and water and saturated ammonium chloride solution were added thereto, followed by extraction using ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and then concentrated to dryness under reduced pressure. The residue was purified using silica gel column chromatography (n-hexane:ethyl acetate=10:1). The solvent was removed under a reduced pressure, giving a yellow oily substance of benzhydrylidene(5-methylbenzofuran-7-yl) amine (17.9 g, yield: 81%).

Source