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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Oxobutanoic Acid | HCID 58 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Aminobenzaldehyde | HCID 68255 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-methylquinoline-2-carboxylate | HCID 20454124 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969376B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-fb5ed0eb7cee4d7db377c33d6d61f0f5 |
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| Source note | uspto-grants-2015_03 |
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