2011International Journal of Engineering Science and TechnologyOpen access

The effective reaction of 2-chloro-3-formylquinoline and acetic acid/sodium acetate under microwave irradiation

Vetrivel Nadaraj, ST Selvi

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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.

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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.

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Available 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.

Key concepts: Acetic acid, Microwave irradiation, Sodium acetate, Chemistry, Nuclear chemistry, Molar ratio, Sodium, Irradiation

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