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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793394Generated: November 3, 2026

Toluene → HCID 23542035, compound

https://huagongshe.com/reaction/1793394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantEthyl 2-aminobenzoateHCID 6877—
Reactant3-Cyclopropyl-3-Oxopropionic Acid Methyl EsterHCID 10130016—
Catalystp-Toluenesulfonic acidHCID 6101—
ProductHCID 23542035HCID 2354203553%

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution of 3-cyclopropyl-3-oxo-propionic acid methyl ester (6.2 g, 0.038 mols), 2-amino benzoic acid ethyl ester (4.95 g, 0.03 mols) and p-toluene sulfonic acid (0.04 g, 0.2 mmols) in toluene (25 ml) was heated at 125° C. for 2 h; 15 ml of solvent was then distilled. To the residual orange solution was added sodium ethoxide (2 M, 15 ml) in ethanol (reaction mixture turns red). This red mixture was stirred at 120° C. for 2 h; 15 ml of solvent was again distilled. The reaction mixture was left to cool to room temperature, diluted with ethyl acetate (1 liter), extracted with HCl 0.1 M and water. The combined organic extracts were dried over sodium sulfate and concentrated in vacuo to leave an orange residue which was washed once with cold ethyl acetate to yield 2-cyclopropyl-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester (3.87 g, 53%) as an off-white solid. LCMS m/z 244.14 [M+H]+ @ RT 0.78 min, 89%, m/z 230.11 [Acid+H]+ @ RT 1.27, 11%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081456B2
Source datasetuspto-grants-2006_07
ORD IDord-9c5e52f4a35d4393b82cadb4af74d145
Source noteuspto-grants-2006_07