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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467518Generated: November 1, 2026

Methanol → Methyl 3-(3-(diethoxymethyl)phenyl)-4-oxo-2-phenyl-1,2,3,4-tetrahydroquinoline-5-carboxylate

https://huagongshe.com/reaction/1467518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl PropionateHCID 7749—
ReactantSodium MethoxideHCID 10942334—
Reactant3-(Diethoxymethyl)benzaldehydeHCID 16217710—
ReactantHCID 178519069HCID 178519069—
ProductMethyl 3-(3-(diethoxymethyl)phenyl)-4-oxo-2-phenyl-1,2,3,4-tetrahydroquinoline-5-carboxylateHCID 6726136325%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of (E)-4-(benzylideneamino)isobenzofuran-1(3H)-one (474 mg, 2 mmol) and 3-(diethoxymethyl)benzaldehyde (418 mg, 2 mmol) in ethyl propionate (20 mL) was cooled to 0° C. Sodium methoxide in methanol solution [sodium (148 mg, 8 mmol) in methanol (2 mL)] was then added dropwise and the mixture was stirred at room temperature overnight. The resulting mixture was evaporated under reduced pressure. The residue was extracted with ethyl acetate (100 mL×3) and the combined organic layers were washed with brine, dried over anhydrous sodium sulfate and concentrated to give crude product. The crude product was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=50:1 to 5:1) to give methyl 3-(3-(diethoxymethyl)phenyl)-4-oxo-2-phenyl-1,2,3,4-tetrahydroquinoline-5-carboxylate (230 mg, yield 25%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999987B2
Source datasetuspto-grants-2015_04
ORD IDord-4955dbe337eb4e21939c062f2bf60793
Source noteuspto-grants-2015_04