HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242028Generated: October 31, 2026
Lithium Hydroxide → 2-Hydroxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid
https://huagongshe.com/reaction/242028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | ethyl 4-methyl-2-oxo-7-(trifluoromethyl)-1H-quinoline-3-carboxylate | HCID 66583605 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 2-Hydroxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid | HCID 66583655 | 88.2% |
Reaction Steps
A 2M aq. LiOH sol. (125 ml) was added to a solution of 15.0 g (50.1 mmol) ethyl 4-methyl-2-oxo-7-(trifluoromethyl)-1H-quinoline-3-carboxylate in a MeOH/THF mixture (175 ml each) and the RS was subsequently heated at 60° C. for 16 h. The mixture was then concentrated in vacuo. The residue was taken up with water and adjusted to pH 2 with a 2M hydrochloric acid, followed by extraction with EtOAc. The organic layer was separated, washed with brine, dried over MgSO4 and concentrated in vacuo. As residue 12.0 g (44.2 mmol, 88%) 4-methyl-2-oxo-7-(trifluoromethyl)-1H-quinoline-3-carboxylic acid was obtained, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653102B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-49ee063805d54042b996741be91c7df9 |
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| Source note | uspto-grants-2014_02 |
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