반응 #43656

ord-79f9c33d2aec480092cc440e638fd2c7

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the mixture was heated
  2. 2
    온도at reflux for 3 h
  3. 3
    농축The mixture was concentrated by rotary evaporation
  4. 4
    기타to yield a solid brown residue
  5. 5
    기타The residue was purified by column chromatography

실험 절차

2-((3-Pyridinyl)methylene)-1-azabicyclo[2.2.2]octan-3-one (6.4 g, 0.024 mol) in dry methanol (45 mL) was added drop-wise to sodium methoxide (produced in situ, 0.036 mol). Nitromethane (3.7 mL, 0.068 mol) was then added, and the mixture was heated at reflux for 3 h. After cooling to room temperature, 1 N HCl was slowly added to adjust pH to 8. The mixture was concentrated by rotary evaporation to yield a solid brown residue. The residue was purified by column chromatography, using ethyl acetate/hexane (1:1, v/v), followed by chloroform/methanol/ammonia (90:10:1, v/v), as eluent, to obtain a yellow oil (4.2 g, 64%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07732607B2uspto-grants-2010_06