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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9329Erstellt: 24. Oktober 2026

Potassium Carbonate → 5-(3-Chloro-phenyl)-3,3-diethyl-1,3-dihydro-indol-2-one

https://huagongshe.com/de/reaction/9329

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt(3-Chlorophenyl)boronic acidHCID 2734323—
Edukt5-Bromo-3,3-diethyl-1,3-dihydro-2H-indol-2-oneHCID 21986250—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt5-(3-Chloro-phenyl)-3,3-diethyl-1,3-dihydro-indol-2-oneHCID 994824627%

Reaktionsschritte

A solution of 5-bromo-1,3-dihydro-3,3-diethyl-[2H]-indol-2-one (2.7 g, 10 mmol), 3-chlorophenylboronic acid (1.6 g, 10 mmol), potassium carbonate (4 g, 30 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.5 g, 0.4 mmol) in dimethoxyethane (100 ml), ethanol (25 ml), and water (25 ml) was heated to reflux for 6 hours. After cooling to room temperature, the mixture was diluted with water and extracted with EtOAc (2×). The combined organic extracts were washed with water, then brine, dried (MgSO4) and evaporated. The residue was purified by column chromatography (SiO2, EtOAc:hexane 1:3) to afford 5-(3-chloro-phenyl)-3,3-diethyl-1,3-dihydro-indol-2-one compound (0.8 g, 27%), m.p. 195–197° C.; 1H-NMR (DMSO-d6) δ 7.70 (t, 1H, J=2 Hz), 7.62–7.60 (m, 1H), 7.58 (d, 1H, J=1.7 Hz), 7.52 (dd, 1H, J=8.1, 2 Hz), 7.43 (t, 1H, J=7.9 Hz), 7.36–7.33 (m, 1H), 6.90 (d, 1H, J=8.1 Hz), 1.87–1.70 (m, 4H) and 0.52 (t, 6H, J=7.4 Hz); MS (+)APCI) m/z 300/302 (M−H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091234B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-6ee58afad1c54d4ca431da562fb42f20
Quellennotizuspto-grants-2006_08