반응 #155317

ord-0bbe72ccf63f4142b91348e1b0ccf454

반응 방정식

Cc1cc(Br)c2occc2c1
7-bromo-5-methylbenzofuran
N=C(c1ccccc1)c1ccccc1
benzophenone imine
CC(C)(C)[O-].[Na+]
sodium t-butoxide
[Cl-].[NH4+]
ammonium chloride
Cc1cc(N=C(c2ccccc2)c2ccccc2)c2occc2c1
benzhydrylidene(5-methylbenzofuran-7-yl) amine
수율 125.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도while heating
  2. 2
    온도under reflux in a nitrogen atmosphere
  3. 3
    추출followed by extraction
  4. 4
    건조The organic layer was dried over anhydrous magnesium sulfate
  5. 5
    농축concentrated to dryness under reduced pressure
  6. 6
    기타The residue was purified
  7. 7
    기타The 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%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE045108E1uspto-grants-2014_09