Moreover, while methylamine, dimethylamine, and trimethylamine increase in basicity corresponding to the introduction of successive methyl groups, phenylamine or aniline, diphenylamine, and triphenylamine are in decreasing order of basicity, the salts of diphenylamine being decomposed by water.
It may be recognized by the blue colour it gives with diphenylamine sulphate and by its reaction with potassium iodide-starch paper.
43) has found that solutions of diphenylamine in methyl cyanide possess an excess of pressure-producing particles and yet are non-conductors of electricity.
Bernthsen (Ann., 1884, 224, p. 1) condensed diphenylamine with fatty acids, in the presence of zinc chloride.
Formic acid yields acridine, and the higher homologues give derivatives substituted at the meso carbon atom, N N +[[Hcooh-C 6 H 5 /Inc6h5->C6h4 C6h4 Cho Ch N N +Ch 3 000h->C 6 H 5 /IC 6 H 5 --C 6 H 4 < >C6h4 Coch 3 C]](CH3) Acridine may also 1:e obtained by passing the vapour of phenylortho-toluidine through a red-hot tube (C. Graebe, Ber., 1884, 17, p. 1 37 0); by condensing diphenylamine with chloroform, in presence of aluminium chloride (0.
The simplest aromatic tertiary amine, triphenylamine, is prepared by the action of brombenzene on sodium diphenylamine (C. Heydrich, Ber., 1885, 18, p. 2156).
Diphenylamine, (C6H5)2NH, is the simplest representative of the true aromatic secondary amines.