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The effective reaction of 2-chloro-3-formylquinoline and acetic acid/sodium acetate under microwave irradiation
Abstract
Pyrano[2,3-b]quinolin-2-ones have been synthesized efficiently from 2-chloro-3-formylquinolines in a single step by treating
with sodium acetate and acetic acid under microwave irradiation. The structures of the compounds have been established by IR,
NMR and mass spectral data. Unexpectedly, 3-formylquinolin-2(1H)-ones were exclusively formed in very high yields by
changing the molar ratio of acetic acid and sodium acetate in just 1.5 to 2.5 min.
with sodium acetate and acetic acid under microwave irradiation. The structures of the compounds have been established by IR,
NMR and mass spectral data. Unexpectedly, 3-formylquinolin-2(1H)-ones were exclusively formed in very high yields by
changing the molar ratio of acetic acid and sodium acetate in just 1.5 to 2.5 min.