Chemistry:Zinin reaction
| Zinin reaction | |
|---|---|
| Named after | Nikolay Zinin |
| Reaction type | Organic redox reaction |
Zinin reaction or Zinin reduction involves reduction of nitro aromatic compounds to the amines using sodium sulfide.[1] It is used to convert nitrobenzenes to anilines.[2][3] The reaction selectively reduces nitro groups in the presence of other easily reduced functional groups (e.g., aryl halides and C=C bonds) are present in the molecule.
Reaction mechanism and example
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 implicated a role for disulfide that is generated in situ. Nitrosobenzenes (ArNO) and phenylhydroxylamine (ArNHOH) are probable intermediates.[4]
Dinitrobenzenes can often be reduced selectively to the nitroaniline. [5]
History
The reaction was discovered by a Russian organic chemist Nikolay Zinin (Russian: Николай Николаевич Зинин) (25 August 1812, Shusha – 18 February 1880, Saint Petersburg).
References
- ↑ Porter, H. K. (1973). "The Zinin Reduction of Nitroarenes". Organic Reactions 20 (4): 455–481. doi:10.1002/0471264180.or020.04. ISBN 0471264180.
- ↑ "Beschreibung einiger neuer organischer Basen, dargestellt durch die Einwirkung des Schwefelwasserstoffes auf Verbindungen der Kohlenwasserstoffe mit Untersalpetersäure" (in German). Journal für Praktische Chemie 27 (1): 140–153. 1842. doi:10.1002/prac.18420270125. https://zenodo.org/record/1427792.
- ↑ Richard Willstätter, Heinrich Kubli (1908). "Über die Reduktion von Nitroverbindungen nach der Methode von Zinin" (in German). Berichte der deutschen chemischen Gesellschaft 41 (2): 1936–1940. doi:10.1002/cber.19080410273. https://zenodo.org/record/1426301.
- ↑ Porter, H. K. (2011), "The Zinin Reduction of Nitroarenes" (in en), Organic Reactions (John Wiley & Sons, Ltd): pp. 455–481, doi:10.1002/0471264180.or020.04, ISBN 978-0-471-26418-7, https://onlinelibrary.wiley.com/doi/abs/10.1002/0471264180.or020.04, retrieved 2022-02-01
- ↑ 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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