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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869573Generated: October 30, 2026

Methanol → Methyl quinoline-6-carboxylate

https://huagongshe.com/reaction/1869573

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 numberUS07638536B2
Source datasetuspto-grants-2009_12
ORD IDord-a2f6dcc1fedb47f3856d98a2ef3fa869
Source noteuspto-grants-2009_12