Production
Aniline is mainly produced in industry in two steps from benzene. First, benzene is nitrated using a concentrated mixture of nitric acid and sulfuric acid at 50 to 60°C, which gives nitrobenzene. In the second step, the nitrobenzene is hydrogenated, typically at 200-300 °C in presence of various metal catalysts:
- C6H5NO2 + 3 H2 → C6H5NH2 + 2 H2O
Originally, the reduction was effected with a mixture of ferrous chloride and iron metal via the Bechamp reduction.
As an alternative, aniline is also prepared from phenol and ammonia, the phenol being derived from the cumene process.
In commerce, three brands of aniline are distinguished: aniline oil for blue, which is pure aniline; aniline oil for red, a mixture of equimolecular quantities of aniline and ortho- and para-toluidines; and aniline oil for safranine, which contains aniline and ortho-toluidine, and is obtained from the distillate (échappés) of the fuchsine fusion.
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