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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815272Generated: October 31, 2026

Ethanol → 5-Phenyloxindole

https://huagongshe.com/reaction/1815272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant5-Bromo-2-oxindoleHCID 611193—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product5-PhenyloxindoleHCID 1330197877.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878733B1
Source datasetuspto-grants-2005_04
ORD IDord-39c674459f2f46f7a0c781e3a22d2a1b
Source noteuspto-grants-2005_04