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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337547Generated: October 26, 2026

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

https://huagongshe.com/reaction/337547

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 numberUS08889718B2
Source datasetuspto-grants-2014_11
ORD IDord-84cd7f2fb6c94d62866527252c9368f3
Source noteuspto-grants-2014_11