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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393283Generated: October 25, 2026

Potassium Carbonate → 3-Ethoxy-2-(4-fluoro-phenyl)-cyclopent-2-enone

https://huagongshe.com/reaction/1393283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Fluorophenylboronic acidHCID 285645—
Reactant2-Bromo-3-ethoxycyclopent-2-enoneHCID 10726911—
CatalystTriphenylphosphineHCID 11776—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-Ethoxy-2-(4-fluoro-phenyl)-cyclopent-2-enoneHCID 2198613970%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Bromo-3-ethoxy-cyclopent-2-enone (Intermediate NINE2) (10.5 g, 51.2 mmol) and K2CO3 (14.2 g, 102 mmol) in toluene (100 mL), benzene (100 mL) and H2O (50 mL) was treated with a solution of 4-fluorophenylboronic acid (9.31 g, 66.5) in EtOH (100 mL). Tetrakis(triphenylphosphine) palladium(0) Pd(PPh3)4 (3 g, 2.6 mmol), bis(dibenzylideneacetone)palladium(0), Pd2(dba)3 (0.47 g, 0.5 mmol) and triphenylphosphine (0.27 g, 1.0 mmol) were added and the mixture was purged with N2 for 15 m. The mixture was heated to 100° C. for 15 h. The mixture was diluted with water and EtOAc:hexane. After extracting with EtOAc:hexane, the combined organic layers were dried over MgSO4, filtered and evaporated to dryness. The crude oil was purified by column chromatography on silica gel with 2.5% EtOAc:CH2Cl2 to give 3-ethoxy-2-(4-fluoro-phenyl)-cyclopent-2-enone (Intermediate NINE3) 7.85 g (70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345077B2
Source datasetuspto-grants-2008_03
ORD IDord-5271b17310ff42c493959161fe4eb708
Source noteuspto-grants-2008_03