Reaktion #7080

Reaktionsgleichung

ammonium chloride

5-bromo-1,3-dihydro-3,3-dimethyl-2H-indol-2-one

3-nitrophenylboronic acid

potassium carbonate

→

title compound

Ausbeute 119.0%

3,3-Dimethyl-5-(3-nitro-phenyl)-1,3-dihydro-indol-2-one

Ausbeute 119.0%

Lösungsmittel

EtOAc

water

dimethoxyethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe reaction was heated
2. 2
   Temperaturto reflux for 2 hours
3. 3
   Filtrationthe mixture was filtered
4. 4
   ExtraktionThe aqueous layer was extracted with ethyl acetate (×2)
5. 5
   Trocknenthe combined organic layers were dried (Na2SO4)
6. 6
   Filtrationfiltered
7. 7
   Sonstigeevaporated
8. 8
   SonstigeThe residue was purified by column chromatography (SiO2, EtOAc: hexane, gradient elution)

Vorschrift

5-bromo-1,3-dihydro-3,3-dimethyl-2H-indol-2-one (1.02 g, 4.26 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.244 g) were stirred under an atmosphere of nitrogen in dimethoxyethane (35 cm3). After 15 minutes, 3-nitrophenylboronic acid (1.43 g, 2.56 mmol) was added, followed by potassium carbonate (3.54 g, 2.56 mmol) in water (15 cm3). The reaction was heated to reflux for 2 hours and then stirred at room temperature overnight. Saturated ammonium chloride and EtOAc were added and the mixture was filtered. The aqueous layer was extracted with ethyl acetate (×2), and then the combined organic layers were dried (Na2SO4), filtered, and evaporated. The residue was purified by column chromatography (SiO2, EtOAc: hexane, gradient elution) to afford the title compound (0.86 g, 67%) mp 234–235° C.; 1H NMR (DMSO-d6) δ 3.33 (s, 6H), 6.98 (d, 1H, J=8.06 Hz), 7.61 (dd, 1H, J=1.85, 8.03 Hz), 7.73 (t, 1H, J=7.98 Hz), 7.81 (d, 1H, J=1.63 Hz), 8.11–8.18 (m, 2H), 8.42–8.43 (m, 1H), 10.5 (s, 1H); MS (EI) m/z 281; Anal. Calc. for C16H14N2O3.0.2H2O: C, 67.51; H, 4.92; N, 9.37; Found: C, 67.48; H, 5.17; N, 9.48.

Quelle