HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242116Generated: October 31, 2026
Lithium Hydroxide → 2-Hydroxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid
https://huagongshe.com/reaction/242116
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 178470056 | HCID 178470056 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 2-Hydroxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid | HCID 66583655 | 88.2% |
Reaction Steps
2M aq. LiOH sol. (125 ml) was added to a solution of 15.0 g (50.1 mmol) 2-hydroxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid ethyl ester in a MeOH/THF mixture (in each case 175 ml) and the solution was subsequently heated to 60° C. for 16 h. The solution was subsequently concentrated in a vacuum. The residue was taken up with water and adjusted to pH 2 with a 2M hydrochloric acid. Extraction was then performed with EtOAc. The organic phase was washed with brine, dried over MgSO4 and concentrated in a vacuum. 12.0 g (44.2 mmol, 88%) 2-hydroxy-4-methyl-7-(trifluoromethyl)quinoline-3-carboxylic acid was obtained as a residue. The raw product was further converted without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653101B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-5ca0920d1c5444d2a55a32c4b1886128 |
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| Source note | uspto-grants-2014_02 |
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