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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874033Generated: October 27, 2026

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

https://huagongshe.com/reaction/1874033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl 2-(4-methoxyphenyl)-3-oxobutanoateHCID 12577863—
Reactant3-Propoxynaphthalen-2-ylamineHCID 21279904—
SolventHexaneHCID 8058—
Product2-(4-methoxyphenyl)-3-methyl-5-propoxy-4H-benzo[f]quinolin-1-oneHCID 5849256372%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304546B2
Source datasetuspto-grants-2012_11
ORD IDord-358f309e2e41412faecb14632ba39d14
Source noteuspto-grants-2012_11