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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1663363Erstellt: 24. Oktober 2026

5-Propylcyclohexane-1,3-dione → 4-[3-Bromo-4-(3-methoxy-benzyloxy)-5-nitro-phenyl]-2-methyl-5-oxo-7-propyl-1,4,5,6,7,8-hexahydro-quinoline-3-carbonitrile

https://huagongshe.com/de/reaction/1663363

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Propylcyclohexane-1,3-dioneHCID 2737224—
Edukt3-AminocrotonitrileHCID 5324720—
Edukt3-Bromo-4-(3-methoxy-benzyloxy)-5-nitro-benzaldehydeHCID 86625158—
LösungsmittelEthanolHCID 702—
Produkt4-[3-Bromo-4-(3-methoxy-benzyloxy)-5-nitro-phenyl]-2-methyl-5-oxo-7-propyl-1,4,5,6,7,8-hexahydro-quinoline-3-carbonitrileHCID 11949649—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 3-bromo-4-(3-methoxy-benzyloxy)-5-nitro-benzaldehyde (50 mg), 3-aminocrotonitrile (13 mg) and 5-propylcyclohexane-1,3-dione (25 mg) in 10 ml of ethanol was stirred at 80° C. for 17 h. The mixture was concentrated in vacuo. The residue was purified by chromatography on silicagel in heptane/ethyl acetate 8/2→1/1 (v/v) as eluent.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08034945B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-9c6cb09aada94387b3abdea5423bd469
Quellennotizuspto-grants-2011_10