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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8208Generated: October 25, 2026

Ethanol → Ethyl 5-fluoropyridine-2-carboxylate

https://huagongshe.com/reaction/8208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDichloromethaneHCID 6344—
ReactantSodium AcetateHCID 517045—
Reactant2-Bromo-5-fluoropyridineHCID 2783171—
ReactantHCID 178418416HCID 178418416—
CatalystPalladium ChlorideHCID 24290—
ProductEthyl 5-fluoropyridine-2-carboxylateHCID 1098667558%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2-bromo-5-fluoropyridine (5.00 g, 28.4 mmol), sodium acetate (9.33 g, 114 mmol), and 1-1′bis(diphenylphosphino)ferrocene]dichloropalladium(II):CH2Cl2 (0.464 g, 0.57 mmol) in ethanol (80 mL) in a Parr® high pressure stainless steel reactor vessel is placed under an atmosphere of 50 psi carbon monoxide and heated at 80-100° C. for 4 h. The vessel is cooled, volatiles removed in vacuo, and the residue partitioned between ethyl acetate and water. The ethyl acetate extract is washed with water and brine, dried over sodium sulfate, filtered, and evaporated to give a dark solid. The residue is chromatographed on SiO2 (10% ethyl acetate/hexanes) to yield the title compound 2.8 g (58%) as a white solid that is recrystallized from hexanes to give white crystals: mp 61-63° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087626B2
Source datasetuspto-grants-2006_08
ORD IDord-61b52ed67bce44c09e6ab3755fd6da79
Source noteuspto-grants-2006_08