HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178Generated: October 23, 2026
2-Pyridone → 5-(4-Chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone
https://huagongshe.com/en/reaction/2178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Pyridone | HCID 8871 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Bromopent-2-yne | HCID 85399 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-Chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone | HCID 18917143 | — |
Reaction Steps
To a suspension of NaH (60% in mineral oil, 200 mg) in dry DMF (50 ml) at 0° C. was added the preceding pyridinone and the mixture was stirred at 0° C. for one half hour. To the resulting suspension was added 1-bromo-2-pentyne dropwise. The resulting mixture was kept at 0° C. during one half hour and poured into saturated aqueous ammonium chloride (200 ml). The aqueous suspension was extracted with ether (3×100 ml) and the combined ether layers washed with brine and dried, yielding the crude product. After column chromatography (silica gel, hexane:ethyl acetate 8:2) the product was obtained as a white amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05728715 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-abf8a35446cd49678e6b7fb0a5cfdc74 |
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| Source note | uspto-grants-1998_03 |
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