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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727461Generated: October 31, 2026

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

https://huagongshe.com/reaction/1727461

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, 1 H), 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 numberUS07495103B2
Source datasetuspto-grants-2009_02
ORD IDord-b2a7262e596545c59a8af6dbfaf56e8a
Source noteuspto-grants-2009_02