1318. The rearrangement of aromatic N-nitroamines. Part V. The acid-catalysed rearrangements of N-nitro-1-naphthylamine and its N-methyl homologue

Abstract

Banthorpe nnd Thomas '7149 1318. The Rearrangement of Aromatic N-Nitroamines. Part V.l The Acid-catalysed Rearrangements of N-Nitro-1 -naphthylarnine and its N-Methyl Homologue

2,4,6-Trimethyl-N-nitroaniline

“…A common feature of primary and secondary N-arylnitramines is their ability to rearrange to the corresponding ortho and para amino±nitro compounds under the in¯uence of an acid (Banthorpe & Thomas, 1965). The molecular structures of N-methyl-N-phenylnitramine and its ring-substituted derivatives are well elucidated.…”