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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422263Generated: October 29, 2026

4-Pentynoic acid ethyl ester → Ethyl 5-(pyridin-2-yl)pent-4-ynoate

https://huagongshe.com/reaction/422263

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Pentynoic acid ethyl esterHCID 143950—
Reactant2-IodopyridineHCID 221126—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductEthyl 5-(pyridin-2-yl)pent-4-ynoateHCID 6659834891.4%

Reaction Steps

In a dry reaction tube containing in suspension copper iodide (60 mg, 0.315 mmol) and triethylamine (17.70 mL, 126 mmol), were added 2-iodopyridine (1.29 g, 6.30 mmol), and the Pd(PPh3)2Cl2 (202 mg, 0.315 mmol). A yellow suspension is obtained and after a few minutes of stirring at room temperature, was added ethyl pent-4-ynoate (790 mg, 6.30 mmol) in solution in 2 mL of triethylamine. Immediately the color of the reaction turns to black. The mixture was stirred at room temperature for 30 min and then at 80° C. for 20 h. Triethylamine was concentrated under reduce pressure and the residue was dissolved in DCM. The organic layer was washed with saturated NH4Cl, water and brine. The solvent was removed under reduced pressure and the crude product was purified by flash chromatography system (prepacked silicagel column 25 g, DCM/MeOH: 98/2 as eluent) to afford 1.17 g of ethyl 5-(pyridin-2-yl)pent-4-ynoate (Yield: 78%) as brownish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-d9489e2e8b974eec978d6bf5aa5eed75
Source noteuspto-grants-2012_01