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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054587Generated: October 30, 2026

Potassium Carbonate → 1-benzyl-5-(4-dibenzofuran-4-yl-phenyl)-3-nitro-1H-pyridin-2-one

https://huagongshe.com/reaction/2054587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-benzyl-5-bromo-3-nitro-1H-pyridin-2-oneHCID 59655962—
Reactant(4-(Dibenzo[b,d]furan-4-yl)phenyl)boronic acidHCID 59655966—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-benzyl-5-(4-dibenzofuran-4-yl-phenyl)-3-nitro-1H-pyridin-2-oneHCID 5965595699.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 1-benzyl-5-bromo-3-nitro-1H-pyridin-2-one (1.0 g, 3.24 mmol), 4-dibenzofuran-4-yl-phenyl-boronic acid (932 mg, 3.24 mmol), K2CO3 (1.34 g, 3 equiv., 9.7 mmol) in toluene (15 mL), ethanol (10 mL) and water (5 mL) was treated with treated with Pd(PPh3)4 (125 mg). After heating to 80° C. overnight, the solution was cooled to room temperature and the resulting solids were filtered and washed with ether (2×6 mL) to give 1-benzyl-5-(4-dibenzofuran-4-yl-phenyl)-3-nitro-1H-pyridin-2-one as a yellow solid (1.53 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329680B2
Source datasetuspto-grants-2008_02
ORD IDord-058a88e42ad747cf89e27b4a7eacd22b
Source noteuspto-grants-2008_02