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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40468Generated: October 25, 2026

Potassium Phosphate, Tribasic → HCID 58502816, compound

https://huagongshe.com/reaction/40468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Bromo-3-methoxycyclopent-2-enoneHCID 11095426—
Reactant4'-Chloro-4-ethylbiphenyl-3-ylboronic acidHCID 59445927—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
ProductHCID 58502816HCID 5850281675.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred suspension of 2-bromo-3-methoxycyclopent-2-enone (1.0 g, 5.23 mmol), 4′-chloro-4-ethylbiphen-3-ylboronic acid (2.03 g, 7.80 mmol) and potassium phosphate (2.23 g, 10.50 mmol) in anhydrous, degassed toluene (25 ml) under an atmosphere of nitrogen is added palladium(II)acetate (24 mg, 0.105 mmol) and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (86 mg, 0.209 mmol). The reaction is heated at 90° C. for 4 hours and then allowed to cool to room temperature, quenched with water (40 ml) and extracted with ethyl acetate (3×30 ml). The organic extracts are combined, washed with brine (15 ml), dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give 2-(4′-chloro-4-ethylbiphen-3-yl)-3-methoxycyclopent-2-enone (1.29 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530388B2
Source datasetuspto-grants-2013_09
ORD IDord-d3c54b276b0a4d53ae8e78a0751849de
Source noteuspto-grants-2013_09