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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893106Generated: October 26, 2026

2-Phenylacetophenone → Benzofurans

https://huagongshe.com/reaction/1893106

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenylacetophenoneHCID 9948—
ReactantCesium carbonateHCID 10796—
Reactant1,2-DibromobenzeneHCID 11414—
ReactantTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
SolventO-XyleneHCID 7237—
ProductBenzofuransHCID 25361380.7%

Reaction Steps

39.2 g of benzyl phenyl ketone, 46.7 g of 1,2-dibromobenzene, g of palladium acetate, 10.5 g of triphenylphosphine, 77.2 g of cesium carbonate, and 400 mL of o-xylene were loaded into a flask, and the mixture was refluxed and stirred under heat under an argon atmosphere for 8 hours. After the completion of the reaction, the reaction solution was filtrated while being extracted with ether. The filtrate was dried with magnesium sulfate, and was then concentrated. The residue was purified by silica gel column chromatography, whereby 43.2 g of a white crystal were obtained (80% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08512875B2
Source datasetuspto-grants-2013_08
ORD IDord-0b22d1ef6f82485cb7e16e9087c5a57c
Source noteuspto-grants-2013_08