반응 #155318

ord-16b0765578604f18b887cc78dc92088b

반응 방정식

Cc1cc(N=C(c2ccccc2)c2ccccc2)c2occc2c1
Benzhydrylidene(5-methylbenzofuran-7-yl)amine
Cl
Hydrochloric acid
[Na+].[OH-]
sodium hydroxide
Cc1cc(N)c2occc2c1
5-methylbenzofuran-7-ylamine

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출followed by extraction
  2. 2
    세척The extract was sequentially washed with an aqueous saturated sodium hydrogen solution
  3. 3
    건조The organic layer was dried over magnesium sulfate
  4. 4
    농축concentrated to dryness under reduced pressure
  5. 5
    기타The residue was purified
  6. 6
    농축The purified product was concentrated to dryness under reduced pressure

실험 절차

Benzhydrylidene(5-methylbenzofuran-7-yl)amine (17.9 g, 0.57 mmol) was dissolved in THF (150 ml). 5N Hydrochloric acid (50 ml) was added thereto, followed by stirring at room temperature for 2 hours. A 5N aqueous sodium hydroxide solution (40 ml) was added to the reaction mixture, followed by extraction using ethyl acetate. The extract was sequentially washed with an aqueous saturated sodium hydrogen solution and an aqueous saturated sodium chloride solution. The organic layer was dried over magnesium sulfate and concentrated to dryness under reduced pressure. The residue was purified using silica gel column chromatography (n-hexane:ethyl acetate=50:1→10:1). The purified product was concentrated to dryness under reduced pressure, giving a dark brown oily substance of 5-methylbenzofuran-7-ylamine (2.5 g, yield: 30%).

출처

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