HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 5-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate → 4-Hydroxy-5-methoxyquinoline-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 5-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 9992162 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-Hydroxy-5-methoxyquinoline-3-carboxylic acid | HCID 45789743 | 52% |
Reaction Steps
A mixture of 5-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester (1 g, 7.1 mmol) in 10% NaOH solution (50 mL) was heated to reflux overnight and then cooled to room temperature. The mixture was extracted with ether. The aqueous phase was separated and acidified with conc. HCl solution to pH 1-2. The resulting precipitate was collected by filtration to give 5-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (A-4) (530 mg, 52%). 1H NMR (DMSO) δ: 15.9 (s, 1H), 13.2 (br, 1H), 8.71 (s, 1H), 7.71 (t, J=8.1 Hz, 1H), 7.18 (d, J=8.4 Hz, 1H), 6.82 (d, J=8.4 Hz, 1H), 3.86 (s, 3H); ESI-MS 219.9 m/z (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829204B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-d46744e7afdd441db71d50f10bdd884a |
| Source note | uspto-grants-2014_09 |