Wolffenstein–Böters reaction

The Wolffenstein–Böters reaction is an organic reaction converting benzene to picric acid by a mixture of aqueous nitric acid and mercury(II) nitrate.[1][2][3] The reaction was discovered by the German chemists Richard Wolffenstein (1864–1929) and Oskar Böters (1848–1912).

According to one series of studies the mercury nitrate first takes benzene to the corresponding nitroso compound and through the diazonium salt to the phenol. The presence of nitrite is essential for the reaction; picric acid formation is prevented when urea, a trap for nitrous acid, is added to the mixture. From then on the reaction proceeds as a regular aromatic nitration.[4][5]

A conceptually related reaction at one time of interest to the pigment industry is the Bohn–Schmidt reaction (1889) involving the hydroxylation of hydroxyantraquinone with sulfuric acid and lead or selenium to a polyhydroxylated anthraquinone.

References

  1. ↑ Wolffenstein and Boeters, Chem. Abs., I, 489, 1861 (1908); 4, 369 (1910);
  2. ↑ Richard Wolffenstein, O. Böters (1913). "Über die katalytische Wirkung des Quecksilbers bei Nitrierungen". Berichte der deutschen chemischen Gesellschaft. 46 (1): 586–589. doi:10.1002/cber.19130460177.
  3. ↑ R. Wolffenstein, W. Paar (1913). "Über Nitrierung der Benzoesäure in Gegenwart von Quecksilber". Berichte der deutschen chemischen Gesellschaft. 46 (1): 589–599. doi:10.1002/cber.19130460178.
  4. ↑ The Mechanism of the Oxynitration of Benzene F. H. Westheimer, Edward Segel, and Richard Schramm J. Am. Chem. Soc.; 1947; 69(4) pp 773 - 785; doi:10.1021/ja01196a011
  5. ↑ The Oxynitration of Benzene. I. Studies Relating to the Reaction MechanismsMarvin Carmack, Manuel M. Baizer, G. Richard Handrick, L. W. Kissinger, and Edward H. Specht J. Am. Chem. Soc.; 1947; 69(4) pp 785 - 790; doi:10.1021/ja01196a012
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