반응 #52681

ord-e32d1bceb1224598860b29e5d8e958ee

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출extracted with ethyl acetate (75 ml)
  2. 2
    세척The combined organic layers were washed with saturated aqueous sodium bicarbonate (50 ml) and brine (50 ml)
  3. 3
    건조The organic layer was dried over magnesium sulfate
  4. 4
    농축concentrated
  5. 5
    기타The resulting solid was triturated with dichloromethane/hexanes

실험 절차

Tetrakis(triphenylphosphine)palladium(0) (0.02 g, 0.02 mmol) was added to a solution of 3-(bromo-4-methoxy-benzylidene)-1,3-dihydroindol-2-one (0.2 g, 0.61 mmol) in toluene (1 ml) and ethanol (1 ml), followed by addition of 2M aqueous sodium carbonate (1.2 ml, 2.4 mmol). To this mixture was added 3-ethoxyphenylboronic acid (0.11 g, 0.67 mmol), and the mixture was held at 100° C. in a sealed tube for 12 hours. The reaction mixture was added to water (40 ml) and extracted with ethyl acetate (75 ml). The combined organic layers were washed with saturated aqueous sodium bicarbonate (50 ml) and brine (50 ml). The organic layer was dried over magnesium sulfate and concentrated. The resulting solid was triturated with dichloromethane/hexanes to afford 0.9 g (39%) of 3-(3′-ethoxy-6-methoxy-biphenyl-3-ylmethylene)-1,3-dihydroindol-2-one as a yellow solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06855730B2uspto-grants-2005_02