HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4,5-dihydroxyquinoline-3-carboxylate → 4,5-Dihydroxyquinoline-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4,5-dihydroxyquinoline-3-carboxylate | HCID 12956450 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4,5-Dihydroxyquinoline-3-carboxylic acid | HCID 15229140 | 87.7% |
Reaction Steps
A mixture of 5-hydroxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester (700 mg, 3 mmol) in 10% NaOH (20 ml) was heated at reflux overnight. After cooling, the mixture was extracted with ether. The aqueous phase was separated and acidified with conc. HCl to pH 1-2. The resulting precipitate was collected via filtration to give 5-hydroxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (A-3) (540 mg, 87%). 1H NMR (DMSO-d6) δ 13.7 (br, 1H), 13.5 (br, 1H), 12.6 (s, 1H), 8.82 (s, 1H), 7.68 (t, J=8.1 Hz, 1H), 7.18 (d, J=8.4 Hz, 1H), 6.82 (d, J=8.4 Hz, 1H); ESI-MS 205.9 m/z (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08741925B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-8cdeca4bd827486e967eaad58128facb |
| Source note | uspto-grants-2014_06 |