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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1507Erstellt: 23. Oktober 2026

2-Pyridone → 5-(4-Chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinone

https://huagongshe.com/de/reaction/1507

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-PyridoneHCID 8871—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Edukt1-Bromopent-2-yneHCID 85399—
EduktEthyl acetate hexaneHCID 21226206—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-(4-Chlorophenyl)-1-(2-pentyn-1-yl)-2-pyridinoneHCID 18917143—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726162
Quelldatensatzuspto-grants-1998_03
ORD IDord-c9ccf1c64cef45c9a38e8ebb2cfb10e4
Quellennotizuspto-grants-1998_03