Zinin reaction
Named after Nikolay Zinin
Reaction type Organic redox reaction

Zinin reaction or Zinin reduction[1] was discovered by a Russian organic chemist Nikolay Zinin (Russian: Николай Николаевич Зинин) (25 August 1812, Shusha – 18 February 1880, Saint Petersburg). This reaction involves conversion of nitro aromatic compounds like nitrobenzene to amines by reduction with sodium sulfides.[2][3] The reaction exhibits excellent selectivity for the nitro group and is useful in cases where other easily reduced functional groups (e.g., aryl halides and C=C bonds) are present in the molecule. Moreover, dinitrobenzenes can often be reduced selectively to the nitroaniline.

Reaction mechanism

Many details of the reaction mechanism are obscure, but it is known that the reaction requires water. Thiosulfate is one product. A possible stoichiometry for the reaction is:

4 ArNO2   +   6 S2-   + 7 H2O → 4  ArNH2   +   3 S2O32- + 6 OH-

Mechanistic studies have shown that disulfide (which is likely to be generated in situ) is a more active reducing agent and may be involved. The reaction is believed to proceed through oxygen transfer to sulfur to give ArNO, followed by further reduction to ArNHOH and, finally, to ArNH2.[4]

Other Examples

  • Reduction of 4,6 (5,7)-dinitro and 5,6-dinitrobenzimidazoles [5]

References

  1. ↑ Porter, H. K. (1973). "The Zinin Reduction of Nitroarenes". Organic Reactions. 20 (4): 455–481. doi:10.1002/0471264180.or020.04. ISBN 0471264180.
  2. ↑ Zinin, N. (1842). "Beschreibung einiger neuer organischer Basen, dargestellt durch die Einwirkung des Schwefelwasserstoffes auf Verbindungen der Kohlenwasserstoffe mit Untersalpetersäure" [Description of some new organic bases, represented by the action of hydrogen sulphide on hydrocarbons with sub-nitric acid]. Journal für Praktische Chemie (in German). 27 (1): 140–153. doi:10.1002/prac.18420270125.
  3. ↑ Richard Willstätter, Heinrich Kubli (1908). "Über die Reduktion von Nitroverbindungen nach der Methode von Zinin" [On the reduction of nitro compounds by the method of Zinin]. Berichte der deutschen chemischen Gesellschaft (in German). 41 (2): 1936–1940. doi:10.1002/cber.19080410273.
  4. ↑ Porter, H. K. (2011), "The Zinin Reduction of Nitroarenes", Organic Reactions, John Wiley & Sons, Ltd, pp. 455–481, doi:10.1002/0471264180.or020.04, ISBN 978-0-471-26418-7, retrieved 2022-02-01
  5. ↑ Sebla Dincer (2002). "The preferential reduction of 4,6 (5,7)-dinitro and 5,6-dinitrobenzimidazoles". Dyes and Pigments. 53 (3): 263–266. doi:10.1016/S0143-7208(02)00018-9.


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