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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525958Generated: October 28, 2026

Sodium → Ethyl 1-ethyl-5,6-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/525958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodiumHCID 5360545—
Reactant1-ethyl-5,6-dimethoxy-1H-benzo[d][1,3]oxazine-2,4-dioneHCID 86732823—
Reactant(Z)-3-ethoxy-3-oxoprop-1-en-1-olateHCID 86732825—
SolventDimethylformamideHCID 6228—
ProductEthyl 1-ethyl-5,6-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 8673282433.9%

Reaction Steps

Under N2, 1-ethyl-5,6-dimethoxy-1H-benzo[d][1,3]oxazine-2,4-dione (12 g, 43.5 mmol) in N,N-Dimethylformamide (DMF) (250 mL) was added to a solution of (Z)-3-ethoxy-3-oxoprop-1-en-1-olate, Sodium salt (18.01 g, 130 mmol) in N,N-Dimethylformamide (DMF) (150 mL) with stirring. The resulting solution was stirred at 110° C. for 3 h. After cooling down, the mixture was concentrated in vacuo and the orange residue was taken up in water. The aqueous solution was washed with ethyl ether (3×), acidified to pH˜2 with 6 N HCl, and extracted with DCM (4×). The organic extracts were dried over Na2SO4, filtered and concentrated. The residue was purified by normal phase silica gel chromatography (CombiFlash), eluting with MeOH/DCM (0-15%) to afford ethyl 1-ethyl-5,6-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate (4.5 g, 14.74 mmol, 33.9% yield) as a brown oil that turned into a brown solid after overnight. LCMS: (M+H)+: 306.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340556B2
Source datasetuspto-grants-2016_05
ORD IDord-67ed1d5c32ca43eabcea7efd539ba8a0
Source noteuspto-grants-2016_05