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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967876Generated: October 26, 2026

Ammonium fluoride → Ethyl 3-(4-pyridyl)furan-2-carboxylate

https://huagongshe.com/reaction/1967876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium fluorideHCID 25516—
Reactant4-(Tri-n-butylstannyl)pyridineHCID 2737318—
ReactantEthyl 3-bromofuran-2-carboxylateHCID 22456149—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(4-pyridyl)furan-2-carboxylateHCID 2314451345.4%

Reaction Steps

Ethyl 3-bromofuran-2-carboxylate (296 mg, 1.35 mmol) obtained in Step 1 of Reference Example 29, 4-(tri-n-butylstannyl)pyridine (550 mg, 1.51 mmol) and tetrakis(triphenylphosphine)palladium(0) (157 mg, 0.136 mmol) were dissolved in THF (10 mL), followed by stirring under heating and reflux for 4 hours. Aqueous ammonium fluoride solution was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was purified through silica gel column chromatography (hexane:ethyl acetate=2:3) to afford ethyl 3-(4-pyridyl)furan-2-carboxylate (133 mg, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420827B2
Source datasetuspto-grants-2013_04
ORD IDord-b2c9eda1d00b4d95a2e9dcd1b51acfed
Source noteuspto-grants-2013_04