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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869722Generated: October 29, 2026

2-Oxobutanoic Acid → Ethyl 3-methylquinoline-2-carboxylate

https://huagongshe.com/reaction/869722

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Oxobutanoic AcidHCID 58—
ReactantSulfuric AcidHCID 1118—
Reactant2-AminobenzaldehydeHCID 68255—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductEthyl 3-methylquinoline-2-carboxylateHCID 20454124—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-aminobenzaldehyde, 2-oxobutyric acid (13.5 g, 132 mmol), and sodium ethoxide (13.5 g, 198 mmol) in ethanol (331 mL) was refluxed for 20 h. After being cooled to 0° C., 96% sulfuric acid (10.6 mL, 97.9 mmol) was added. The reaction mixture was refluxed for 20 h. After being cooled to 0° C., the reaction mixture was basified to pH 8-9 with saturated sodium bicarbonate, and the mixture was extracted with chloroform. The organic layer was washed with water and saturated brine, dried over sodium sulfate, filtrated and concentrated in vacuo. The crude was purified by silica gel column chromatography (hexane:ethyl acetate=19:1 to 2:1) to give ethyl 3-methylquinoline-2-carboxylate. MS (APCI): m/z 218 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969376B2
Source datasetuspto-grants-2015_03
ORD IDord-fb5ed0eb7cee4d7db377c33d6d61f0f5
Source noteuspto-grants-2015_03