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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560144Generated: October 25, 2026

Potassium Carbonate → 4-(2-Methyl-5-oxo-1-cyclopenten-1-yl)benzonitrile

https://huagongshe.com/reaction/560144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant4-Cyanophenylboronic acidHCID 2734326—
Reactant2-Bromo-3-methyl-2-cyclopenten-1-oneHCID 4437009—
Catalyst1,5-Diphenylpenta-1,4-dien-3-one;palladiumHCID 154270—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product4-(2-Methyl-5-oxo-1-cyclopenten-1-yl)benzonitrileHCID 21986159—

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Bromo-3-methyl-cyclopent-2-enone (Intermediate TEN1) (commercially available from Aldrich) (2.04 g, 11.4 mmol) and K2CO3 (3.16 g in 11 mL H2O) in toluene (45 mL) was treated with a solution 4-cyanophenylboronic acid (commercially available from Aldrich) (2.2 g, 15 mmol) in EtOH (27 mL). Tetrakis(triphenylphosphine) palladium(0) Pd(PPh3)4 (0.4 g), bis(dibenzylideneacetone) palladium(0), Pd2(dba)3 (0.055 g, ˜5 mol %) and triphenylphosphine (0.4 g) were added and the mixture was purged with N2 for 15 m. The mixture was heated to 80° 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 CH2Cl2 to give 4-(2-methyl-5-oxo-cyclopent-1-enyl)-benzonitrile (Intermediate TEN2) 1.74 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063086B2
Source datasetuspto-grants-2011_11
ORD IDord-721c357b58a744988bc9f8318b4c2bd4
Source noteuspto-grants-2011_11