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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368402Generated: October 31, 2026

Ethanol → 5-Phenyloxindole

https://huagongshe.com/reaction/1368402

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 numberUS06573293B2
Source datasetuspto-grants-2003_06
ORD IDord-8b07ea2c4c504ddf81153f6e8c02fc4e
Source noteuspto-grants-2003_06