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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68141Erstellt: 24. Oktober 2026

Benzene → HCID 58492563, Verbindung

https://huagongshe.com/de/reaction/68141

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzeneHCID 241—
EduktEthyl AcetateHCID 8857—
EduktEthyl 2-(4-methoxyphenyl)-3-oxobutanoateHCID 12577863—
Edukt3-Propoxynaphthalen-2-ylamineHCID 21279904—
LösungsmittelHexaneHCID 8058—
ProduktHCID 58492563HCID 5849256372%

Reaktionsschritte

To a benzene solution (38 ml) containing 3-propoxynaphthalen-2-ylamine (600 mg, 2.98 mmol) and ethyl α-acetyl-4-methoxyphenylacetate (1.41 g, 5.96 mmol) was added 85 mg of Amberlyst 15 (Sigma-Aldrich). The resulting mixture was heated under reflux for 20 hours using a Dean-Stark trap. The reaction mixture was cooled to room temperature, filtered to remove resin, and then the filtrate was concentrated under reduced pressure. Diphenyl ether (2.8 ml) was added to the residue, and the mixture was then heated with a mantle heater and stirred for 70 minutes under reflux. The resulting reaction mixture was cooled to room temperature, and then directly purified using silica gel column chromatography (dichloromethane:methanol=80:1→70:1). The purified product was concentrated under reduced pressure, giving an oily substance (800 mg, yield: 72%). Ethyl acetate and n-hexane were added to the thus-obtained oily substance to crystallize and then recrystallized from ethyl acetate, giving a pale yellow powder of 2-(4-methoxyphenyl)-3-methyl-5-propoxy-4H-benzo[f]quinolin-1-one (290 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE045108E1
Quelldatensatzuspto-grants-2014_09
ORD IDord-bd794614aa9f415481ca693716300b61
Quellennotizuspto-grants-2014_09