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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577176Generated: October 28, 2026

Ethyl 3-bromo-5-fluoropyridine-4-carboxylate → HCID 59589366, compound

https://huagongshe.com/reaction/577176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-bromo-5-fluoropyridine-4-carboxylateHCID 46311470—
ReactantHCID 178418750HCID 178418750—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59589366HCID 5958936651%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of ethyl 3-bromo-5-fluoropyridine-4-carboxylate (4.8 g, 20 mmol) in anhydrous 1,4-dioxane (30 mL) at room temperature was added (1,1′-bis(diphenylphosphino)ferrocene)dichloropalladium (II) (325 mg, 0.43 mmol), followed by a diethylzinc solution (22 mL, 20 mmol, 1.1 M solution in toluene). The mixture was stirred at 70° C. for 45 minutes. After cooling to room temperature, the reaction was quenched with MeOH. Ethyl acetate (100 mL) was added. The mixture was extracted with 0.1 N HCl (200 mL). The organic layer was recovered. The pH of the aqueous phase was brought to 6 with 2 N NaOH. The mixture was extracted with EtOAc (1×100 mL). The combined organic extracts were dried over MgSO4, filtered, evaporated, and dried in vacuo. The crude product was purified by flash chromatography (0-20% ethyl acetate/hexane), affording ethyl 3-ethyl-5-fluoropyridine-4-carboxylate (2.0 g, 51% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040538B2
Source datasetuspto-grants-2015_05
ORD IDord-0c3346e332434df98ab0a31bc97fe2e8
Source noteuspto-grants-2015_05