반응 #155317
ord-0bbe72ccf63f4142b91348e1b0ccf454
반응 방정식
용매
반응 조건
후처리
- 1온도while heating
- 2온도under reflux in a nitrogen atmosphere
- 3추출followed by extraction
- 4건조The organic layer was dried over anhydrous magnesium sulfate
- 5농축concentrated to dryness under reduced pressure
- 6기타The residue was purified
- 7기타The solvent was removed under a reduced pressure
실험 절차
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%).