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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49121Erstellt: 25. Oktober 2026

Ethanol → 5-Phenyloxindole

https://huagongshe.com/reaction/49121

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium CarbonateHCID 10340—
EduktPhenylboronic AcidHCID 66827—
Edukt5-Bromo-2-oxindoleHCID 611193—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-PhenyloxindoleHCID 1330197877,3%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

5-Bromo-2-oxindole (5 g, 23.5 mmol) was dissolved in 110 mL of toluene and 110 mL of ethanol with stirring and a little heating. Tetrakis(triphenylphosphine)-palladium(0) (1.9 g, 1.6 mmol) was added followed by a 2M aq. solution of sodium carbonate (40 mL, 80 mmol). To this mixture benzene boronic acid (3.7 g, 30.6 mmol) was added and the mixture was heated in a 100° C. oil bath. After 12 h, the reaction was diluted with ethyl acetate (500 mL), washed with saturated aq. sodium bicarbonate (200 mL), water (200 mL), 1N HCl (200 mL) and brine (200 mL). The organic layer was dried with magnesium sulfate and concentrated to afford a brown solid. Trituration with dichloromethane and filtering afforded 3.8 g (77%) of a tan solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06706709B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-53c59fa6a8fe410f8728af630b8a9eb8
Quellennotizuspto-grants-2004_03