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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931376Generated: October 31, 2026

Potassium Carbonate → Ethyl 5-bromo-2-(2-nitropyridin-3-yl)-3-oxo-2,3-dihydro-1-benzofuran-2-carboxylate

https://huagongshe.com/reaction/931376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluoro-2-nitropyridineHCID 2762802—
ReactantEthyl 5-bromo-3-oxo-2,3-dihydro-1-benzofuran-2-carboxylateHCID 58458886—
SolventDimethyl SulfoxideHCID 679—
ProductEthyl 5-bromo-2-(2-nitropyridin-3-yl)-3-oxo-2,3-dihydro-1-benzofuran-2-carboxylateHCID 58458882—

Reaction Conditions

Temperature87.5 °C

Reaction Steps

A mixture of ethyl 5-bromo-3-oxo-2,3-dihydro-1-benzofuran-2-carboxylate (1.42 g, 5.0 mmol), 2-nitro-3-fluoropyridine (0.71 g, 5 mmol) and potassium carbonate (0.83 g, 6.0 mmol) in DMSO (15 mL) is heated at 85-90° C. for 18 h. The mixture is cooled to ambient temperature and partitioned between EtOAc and brine. The layers are separated and the aqueous layer is further extracted with EtOAc. The combined organic extracts are dried (Na2SO4), filtered and concentrated in vacuo. The residue is purified by silica gel chromatography (gradient elution with hexanes-EtOAc) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296750B2
Source datasetuspto-grants-2016_03
ORD IDord-3e8ea1c00e014b29a6944455a9b9c773
Source noteuspto-grants-2016_03