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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridoneHCID 8871—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Bromopent-2-yneHCID 85399—
ReactantEthyl acetate hexaneHCID 21226206—
SolventDimethylformamideHCID 6228—
Product5-(4-Chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinoneHCID 18917143—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728715
Source datasetuspto-grants-1998_03
ORD IDord-abf8a35446cd49678e6b7fb0a5cfdc74
Source noteuspto-grants-1998_03