Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051114Generated: November 1, 2026

Toluene → 5-(3-fluorophenyl)benzofuran-3(2H)-one

https://huagongshe.com/reaction/1051114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantCesium carbonateHCID 10796—
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant5-Bromobenzo[b]furan-3(2H)-oneHCID 10512748—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Product5-(3-fluorophenyl)benzofuran-3(2H)-oneHCID 11816155799%

Reaction Conditions

Temperature80 °C

Reaction Steps

Cesium carbonate (612 mg, 1.88 mmol) was added to a solution of 5-bromobenzofuran-3(2H)-one (200 mg, 0.939 mmol), (3-fluorophenyl)boronic acid (263 mg, 1.88 mmol) and toluene (20 mL) in a 50 mL Schlenk tube. A nitrogen atmosphere was established by evacuating and refilling with nitrogen (3×), then tetrakis(triphenylphosphine)palladium (0) (11 mg, 0.01 mmol) was added to the reaction. The flask was sealed and heated in a 80° C. oil bath overnight. The resulting mixture was cooled to room temperature. The reaction was then diluted with ethyl acetate and filtered through celite. Ethyl acetate (30 mL) was used to wash the flask and the combined organic filtrate was concentrated. The resulting crude residue was purified on a Teledyne-Isco Combiflash machine (40 g column, hexanes→100% ethyl acetate/hexanes, gradient), to afford 212 mg (99%) of 5-(3-fluorophenyl)benzofuran-3(2H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388153B2
Source datasetuspto-grants-2016_07
ORD IDord-8d6a00830e8642d39928acf51cf52f8f
Source noteuspto-grants-2016_07