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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2123Erstellt: 23. Oktober 2026

2-Hydroxyquinoline → 5-Chloro-1-(2-pentyn-1-yl)-2-quinolinone

https://huagongshe.com/de/reaction/2123

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-HydroxyquinolineHCID 6038—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Edukt1-Bromopent-2-yneHCID 85399—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelHexaneHCID 8058—
Produkt5-Chloro-1-(2-pentyn-1-yl)-2-quinolinoneHCID 18917094—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a suspension of NaH (60% in mineral oil, 700 mg) in dry DMF (100 ml) at 0° C. was added the preceding quinolinone (2.05 g) and the mixture was stirred at 0° C. for one half hour. To the resulting suspension was added 1-bromo-2-pentyne (1.6 g) dropwise. The resulting mixture was kept at 0° C. for one half hour and poured into saturated aqueous ammonium chloride (200 ml). The aqueous suspension was extracted with ether (3×100 ml), the combined ether layers washed with brine and dried, yielding the crude product. Trituration with hexane yielded the product as a yellow solid (1 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05728698
Quelldatensatzuspto-grants-1998_03
ORD IDord-3d045ba7bb254c15a155333d94ac21c7
Quellennotizuspto-grants-1998_03