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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Pentynoic acid ethyl ester | HCID 143950 | — |
| Reactant | 2-Iodopyridine | HCID 221126 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 5-(pyridin-2-yl)pent-4-ynoate | HCID 66598348 | 91.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101637B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-d9489e2e8b974eec978d6bf5aa5eed75 |
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| Source note | uspto-grants-2012_01 |
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