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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196483Generated: October 31, 2026

Methanol → Methyl quinoline-6-carboxylate

https://huagongshe.com/reaction/2196483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfate IonHCID 1117—
Reactant6-Quinolinecarboxylic acidHCID 82571—
ProductMethyl quinoline-6-carboxylateHCID 736812—

Reaction Conditions

Temperature70 °C

Reaction Steps

4.0 g of 6-quinolinecarboxylic acid were suspended in 30 ml of MeOH, 2.0 ml of conc. sulfate was added under ice cooling, and the mixture was stirred at 70° C. for 22 hours. The reaction solution was concentrated under reduced pressure, and the residue was mixed with water and neutralized with potassium carbonate. The thus-precipitated solid was filtered and dried to obtain 4.28 g of 6-quinolinecarboxylic acid methyl ester. 0.5 g of the obtained ester body was dissolved in 5 ml of formamide, 0.15 ml of conc. sulfate, 0.05 g of ferrous sulfate hepta-hydrate, and 0.4 ml of 31% hydrogen peroxide were sequentially added thereto, and the mixture was stirred at 80° C. for 50 minutes. The reaction solution was mixed with water and alkalinized with potassium carbonate. 10% MeOH-chloroform was added, and insoluble matter was filtered using celite. The obtained filtrate was separated, the obtained organic layer was dried over anhydrous sodium sulfate and concentrated, and the obtained residue was washed with EtOH to obtain 0.15 g of 6-methoxycarbonyl-2-quinolinecarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338429B2
Source datasetuspto-grants-2012_12
ORD IDord-4d74227129dc4ca0a86e55a39f997f82
Source noteuspto-grants-2012_12