The reaction of bis(2-pyridyl)amine with nitric acid (50% molar excess) in sulfuric acid results in complete conversion of the substrate into mono-, di-, and trinitro derivatives which were identified by IR, NMR, and mass spectra and X-ray analysis. A mechanism was proposed for easy nitration of such a fairly basic substrate in strongly acidic medium.

New study of the reaction of bis(2-pyridyl)amine with nitric acid

VERARDO, Giancarlo;TOLAZZI, Marilena;
2000-01-01

Abstract

The reaction of bis(2-pyridyl)amine with nitric acid (50% molar excess) in sulfuric acid results in complete conversion of the substrate into mono-, di-, and trinitro derivatives which were identified by IR, NMR, and mass spectra and X-ray analysis. A mechanism was proposed for easy nitration of such a fairly basic substrate in strongly acidic medium.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11390/708459
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