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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40480Generated: October 25, 2026

Cesium fluoride → 2-(2',4'-Dichloro-4-cyclopropylbiphenyl-3-yl)-cyclopentane-1,3-dione

https://huagongshe.com/reaction/40480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant(2,4-Dichlorophenyl)boronic acidHCID 2734659—
Reactant2-(5-Bromo-2-cyclopropylphenyl)cyclopentane-1,3-dioneHCID 66676860—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(2',4'-Dichloro-4-cyclopropylbiphenyl-3-yl)-cyclopentane-1,3-dioneHCID 66991468—

Reaction Conditions

Temperature160 °C

Reaction Steps

To a mixture of 2-(5-bromo-2-cyclopropylphenyl)cyclopentane-1,3-dione (0.100 g, 0.34 mmol), 2,4-dichlorophenylboronic acid (0.090 g, 0.47 mmol), [1,1′-bis(diphenylphosphino)-ferrocene]palladium(II)chloride (22 mg, 0.027 mmol) and cesium fluoride (0.152 g, 1.0 mmol) is added 1,2-dimethoxyethane (1 ml). After evacuating and flushing with nitrogen (×3) the mixture is heated at 160° C. for 15 minutes under microwave irradiation. After dilution with distilled water the crude product is extracted with ethyl acetate (×3), and the organic phase is washed with brine, dried over magnesium sulfate and concentrated in vacuo. The crude product is then purified by flash column chromatography on silica gel (isohexane/ethyl acetate eluant) and further triturated with hexanes to afford 2-(2′,4′-dichloro-4-cyclopropylbiphenyl-3-yl)-cyclopentane-1,3-dione as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530388B2
Source datasetuspto-grants-2013_09
ORD IDord-f9debeb7e7ec4267bfd5613e8c24221f
Source noteuspto-grants-2013_09