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122224-58-2

6,7-Dichloro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid Ethyl Ester synthesis

4synthesis methods
-

Yield:122224-58-2 63 %

Reaction Conditions:

in 1,4-dioxane;Reflux;

Steps:

Ethyl 6-fluoro-1,4-dihydroquinoline-4-one-3-carboxylate (3a).

General procedure: A mixture of aniline 1 (0.01 mol) and diethyl 2-(ethoxymethylene)malonate (0.1 mol) was taken in 20 mL of dioxane and heated and stirred at reflux for 9 h. The reaction mixture was allowed to cool at room temperature and poured in ice-cooled water. The precipitated product dried under a vacuum and recrystallized from absolute alcohol. Ethyl 6-fluoro-1,4-dihydroquinoline-4-one-3-carboxylate (3a).

References:

Dubal;Vachchharajani;Solanki;Shah [Russian Journal of General Chemistry,2022,vol. 92,# 10,p. 2161 - 2168][Zh. Obshch. Khim.,2022,vol. 92,# 10,p. 2161 - 2168]