Issue 18, 1972

The mechanism of bromination of pyrimidin-2(1H)-one, its N-methyl and NN′-dimethyl derivatives

Abstract

Bromination at the 5-position of the title compounds in aqueous sulphuric acid solutions involves rapid formation of an addition compound which undergoes slow acid-catalysed elimination to form the substitution product, which in turn may react further with an excess of bromine.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 1032-1033

The mechanism of bromination of pyrimidin-2(1H)-one, its N-methyl and NN′-dimethyl derivatives

O. S. Tee and S. Banerjee, J. Chem. Soc., Chem. Commun., 1972, 1032 DOI: 10.1039/C39720001032

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