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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Fluoro-2-nitropyridine | HCID 2762802 | — |
| Reactant | Ethyl 5-bromo-3-oxo-2,3-dihydro-1-benzofuran-2-carboxylate | HCID 58458886 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl 5-bromo-2-(2-nitropyridin-3-yl)-3-oxo-2,3-dihydro-1-benzofuran-2-carboxylate | HCID 58458882 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09296750B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-3e8ea1c00e014b29a6944455a9b9c773 |
|---|
| Source note | uspto-grants-2016_03 |
|---|