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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406736Generated: October 25, 2026

Phenol → 3-Nitrobenzofuro[2,3-b]pyridine

https://huagongshe.com/reaction/2406736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPotassium CarbonateHCID 11430—
ReactantDimethylacetamideHCID 31374—
Reactant3-Bromo-2-chloro-5-nitropyridineHCID 230889—
Catalyst3375-31-3HCID 58759193—
SolventWaterHCID 962—
Product3-Nitrobenzofuro[2,3-b]pyridineHCID 6861906552.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

Potassium carbonate (87 mg) and phenol (47 mg) were added to an N,N-dimethylacetamide (1 ml) solution containing 3-bromo-2-chloro-5-nitropyridine (100 mg), followed by stirring at 70° C. for 3 hours. Acetic acid palladium (20 mg) was added in a nitrogen atmosphere, followed by stirring at 100° C. for 3.5 hours. Water was added, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate. Subsequently, the solvent was distilled away under reduced pressure, hexane and ethyl acetate were added to the obtained residue, an insoluble precipitate was collected by filtration, and a light yellow solid of 3-nitrobenzofuro[2,3-b]pyridine (47.1 mg) was thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809371B2
Source datasetuspto-grants-2014_08
ORD IDord-50655dca60054437842f1787d66784bb
Source noteuspto-grants-2014_08