Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230771Generated: October 25, 2026

Triethylamine → Ethyl 5-Chloropyridine-2-carboxylate

https://huagongshe.com/reaction/230771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-5-chloropyridineHCID 817098—
ReactantN,N-dimethylformamide ethanolHCID 19794673—
ReactantHCID 178418416HCID 178418416—
Catalystpalladium(II) acetateHCID 167845—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
ProductEthyl 5-Chloropyridine-2-carboxylateHCID 15414989—

Reaction Steps

Palladium acetate (117 mg), 1,1′-bis(diphenylphosphino)ferrocene (577 mg) and triethylamine (1.4 mL) were added to an ethanol-DMF mixed solvent (1/1, 30 mL) of 2-bromo-5-chloropyridine (1.0 g), and stirred overnight in a carbon monoxide atmosphere (1 atmospheric pressure) at 50° C. Ethanol was evaporated off under reduced pressure from the reaction solution, water was added to the resulting residue, and extracted with hexane/ethyl acetate (2/3). The organic layer was dried with anhydrous magnesium sulfate, and the solvent was evaporated off under reduced pressure. The resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=9/1 to 4/1) to obtain the entitled compound (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566781B2
Source datasetuspto-grants-2009_07
ORD IDord-3357ba49289043cfb599c5ea7e8e0095
Source noteuspto-grants-2009_07