반응 #45555

ord-ff74efec60a34a189d6388ef3f692111

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도by refluxing with a Dean-Stark condenser for 2.5 hours
  2. 2
    온도After cooling
  3. 3
    추출the product was extracted with ethyl acetate (30 ml×2)
  4. 4
    세척The organic layer was washed with saturated brine (30 ml)
  5. 5
    건조dried over anhydrous magnesium sulfate
  6. 6
    농축concentrated under reduced pressure
  7. 7
    기타the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=8:1)

실험 절차

Toluene (3 ml), p-toluenesulfonic acid monohydrate (1.4 mg, 7.5 μmol) were added to N-(3-bromo-6-cyano-2-hydroxy-5-methyl-4-styrylphenyl)-2,2-dimethylpropionamide (I-14) (31 mg, 75 μmol), followed by refluxing with a Dean-Stark condenser for 2.5 hours. After cooling, saturated sodium bicarbonate water (30 ml) was added to the reaction liquid, the product was extracted with ethyl acetate (30 ml×2). The organic layer was washed with saturated brine (30 ml), dried over anhydrous magnesium sulfate, concentrated under reduced pressure, the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=8:1) to obtain the entitled compound (25 mg, 84%) as a colorless solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07737166B2uspto-grants-2010_06