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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401225Generated: October 30, 2026

Sodium Acetate → Ethyl 5-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/401225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant8-bromo-4-hydroxy-5-methoxy-3-Quinolinecarboxylic acid ethyl esterHCID 10245802—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductEthyl 5-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 999216257%

Reaction Steps

A mixture of 8-bromo-5-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester (2.3 g, 7.1 mmol), sodium acetate (580 mg, 7.1 mmol) and 10% Pd/C (100 mg) in glacial acetic acid (50 ml) was stirred under H2 (2.5 atm) overnight. The catalyst was removed via filtration, and the reaction mixture was concentrated under reduced pressure. The resulting oil was dissolved in CH2Cl2 (100 mL) and washed with aqueous sodium bicarbonate solution and water. The organic layer was dried, filtered and concentrated. The crude product was purified by column chromatography to afford 5-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester as a yellow solid (1 g, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741925B2
Source datasetuspto-grants-2014_06
ORD IDord-cd1ea30864344e22bd66f99e42c5d43c
Source noteuspto-grants-2014_06