Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915220Generated: November 2, 2026

Ethyl 5-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate → 4-Hydroxy-5-methoxyquinoline-3-carboxylic acid

https://huagongshe.com/reaction/1915220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 9992162—
SolventSodium HydroxideHCID 14798—
Product4-Hydroxy-5-methoxyquinoline-3-carboxylic acidHCID 4578974352%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614327B2
Source datasetuspto-grants-2013_12
ORD IDord-dc5bd6bf184a499285c0d39e6bb9cf91
Source noteuspto-grants-2013_12