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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1474526Erstellt: 25. Oktober 2026

3-Propoxynaphthalen-2-ylamine → 2-(4-methoxyphenyl)-5-propoxy-4H-benzo[f]quinolin-1-one

https://huagongshe.com/reaction/1474526

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Propoxynaphthalen-2-ylamineHCID 21279904—
EduktEthyl alpha-(hydroxymethylene)-4-methoxyphenylacetateHCID 67418551—
LösungsmittelBenzeneHCID 241—
Produkt2-(4-methoxyphenyl)-5-propoxy-4H-benzo[f]quinolin-1-oneHCID 4622439742,4%

Reaktionsschritte

To a benzene solution (50 ml) containing 3-propoxynaphthalen-2-ylamine (2.05 g, 10.18 mmol) and ethyl α-(hydroxymethylene)-4-methoxyphenylacetate (2.29 g, 10.3 mmol) was added 350 mg of Amberlyst 15 (Sigma-Aldrich). The resulting mixture was heated under reflux for 21 hours using a Dean-Stark trap. The reaction mixture was then cooled to room temperature, filtered to remove resin, and then the filtrate was concentrated under reduced pressure. Diphenyl ether (2.2 ml) was added to the residue, and the mixture was then heated with a mantle heater and stirred for 1.5 hours under reflux. The resulting reaction mixture was cooled to room temperature, and then directly purified using silica gel column chromatography (dichloromethane:methanol=100:1→60:1). The purified product was concentrated under reduced pressure to recrystallize the residue from ethyl acetate-n-hexane, giving a pale yellow powder of 2-(4-methoxyphenyl)-5-propoxy-4H-benzo[f]quinolin-1-one (1.55 g, yield: 42%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09018229B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-9d50674f6cee4365b46efb8c17a517db
Quellennotizuspto-grants-2015_04