HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194505Generated: October 25, 2026
Water → 1-Methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid
https://huagongshe.com/reaction/2194505
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylate | HCID 67009555 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-Methyl-2-oxo-1,2-dihydroquinoline-3-carboxylic acid | HCID 12415351 | 96% |
Reaction Steps
2.4 g (10.4 mmol) of ethyl 1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylate was dissolved in 1,4-dioxane (50 mL), and 0.65 g (15 mmol) of lithium hydroxide monohydrate and 10 mL of water were added to the solution at room temperature. The resulting mixture was stirred for 24 hours at room temperature. The reaction mixture was poured into an aqueous solution of sodium hydrogen carbonate, and the mixture was washed with ethyl acetate. The aqueous phase was acidified with citric acid, and then the mixture was extracted with chloroform. The organic phase was washed with water, dried, and concentrated. The residue thus obtained was washed with ethyl acetate, and thus 2.02 g (yield: 96%) of the title compound was obtained as light yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08334236B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-8f720b76a6684cdfb885a540b9da2f49 |
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| Source note | uspto-grants-2012_12 |
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