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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49122Erstellt: 24. Oktober 2026

Ethanol → 6-Pyridin-3-yl-1,3-dihydro-indol-2-one

https://huagongshe.com/de/reaction/49122

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium CarbonateHCID 10340—
Edukt6-bromo-2,3-dihydro-1H-indol-2-oneHCID 2773289—
EduktPyridine-3-boronic acid propane diolHCID 69587225—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
Produkt6-Pyridin-3-yl-1,3-dihydro-indol-2-oneHCID 2191557942%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 6-bromo-2-oxindole (4 g, 26.3 mmol) dissolved in 60 mL of toluene and 60 mL of ethanol with stirring and a little heating tetrakis(triphenyl-phosphine)palladium(0) (2.3 g, 1.9 mmol) was added followed by a 2M aqueous solution of sodium carbonate (50 mL, 100 mmol) and pyridine-3-boronic acid propane diol (5 g, 30.7 mmol). The mixture was heated in a 100° C. oil bath for 12 hours. The cooled reaction was diluted with ethyl acetate (500 mL), washed with saturated aqueous sodium bicarbonate (200 mL), water (200 mL) and brine (200 mL). The organic layer was dried with magnesium sulfate and concentrated to afford a brown solid. The residue was triturated with methylene chloride/diethyl ether to give 2.32 g (42%) of 6-pyridin-3-yl-1,3-dihydro-indol-2-one as a brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06706709B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-c51a563b1d5e48e99b901ce71d587a2a
Quellennotizuspto-grants-2004_03