Chemistry:Reduction of nitro compounds

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Short description: Chemical reaction

The reduction of nitro compounds are chemical reactions of wide interest in organic chemistry. The conversion can be effected by many reagents. The nitro group was one of the first functional groups to be reduced. Alkyl and aryl nitro compounds behave differently. Most useful is the reduction of aryl nitro compounds.

Aromatic nitro compounds

Reduction to anilines

Generalization of the reduction of a nitroarene to aniline

The reduction of nitroaromatics is conducted on an industrial scale.[1] Many methods exist, such as:

Metal hydrides are typically not used to reduce aryl nitro compounds to anilines because they tend to produce azo compounds. (See below)

Reduction to hydroxylamines

Several methods have been described for the production of aryl hydroxylamines from aryl nitro compounds:

Reduction to hydrazine compounds

Treatment of nitroarenes with excess zinc metal results in the formation of N,N'-diarylhydrazine.[19]

Reduction to azo compounds

Generalization of the reduction of a nitroarene to an azo compound

Treatment of aromatic nitro compounds with metal hydrides gives good yields of azo compounds. For example, one could use:

Aliphatic nitro compounds

Reduction to hydrocarbons

Generalization of the reduction of a nitroalkane to an alkane

Hydrodenitration (replacement of a nitro group with hydrogen) is difficult to achieve but can be effected by catalytic hydrogenation over platinum on silica gel at high temperatures.[21] The reaction can also be effected through radical reaction with tributyltin hydride and a radical initiator, AIBN as an example.[22]

Reduction to amines

Generalization of the reduction of a nitroalkane to an amine

Aliphatic nitro compounds can be reduced to aliphatic amines by several reagents:

α,β-Unsaturated nitro compounds can be reduced to saturated amines by:

Reduction to hydroxylamines

Aliphatic nitro compounds can be reduced to aliphatic hydroxylamines using diborane.[30]

Generalization of the reduction of a nitroalkane to a hydroxylamine

The reaction can also be carried out with zinc dust and ammonium chloride:[31][32][33]

R-NO2 + 4 NH4Cl + 2 Zn → R-NH-OH + 2 ZnCl2 + 4 NH3 + H2O

Reduction to oximes

Generalization of the reduction of a nitroalkane to an oxime

Nitro compounds are typically reduced to oximes using metal salts, such as tin(II) chloride[34] or chromium(II) chloride.[35] Additionally, catalytic hydrogenation using a controlled amount of hydrogen can generate oximes.[36]

References

  1. ↑ Gerald Booth (2007). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_411. 
  2. ↑ Allen, C. F. H.; VanAllan, J. (1955). "2-Amino-p-cymene". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv3p0063. ; Collective Volume, 3, pp. 63 
  3. ↑ Bavin, P. M. G. (1973). "2-Aminofluorene". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv5p0030. ; Collective Volume, 5, pp. 30 
  4. ↑ Smith, Michael B.; March, Jerry (2007). March's Advanced Organic Chemistry (6th ed.). John Wiley & Sons. p. 1816. ISBN 978-0-471-72091-1. 
  5. ↑ Ram, Siya; Ehrenkaufer, Richard E. (1984). "A general procedure for mild and rapid reduction of aliphatic and aromatic nitro compounds using ammonium formate as a catalytic hydrogen transfer agent". Tetrahedron Letters 25 (32): 3415–3418. doi:10.1016/S0040-4039(01)91034-2. 
  6. ↑ 6.0 6.1 Adams, J. P. (2002). "Nitro and related groups" (in en). Journal of the Chemical Society, Perkin Transactions 1 (23): 2586–2597. doi:10.1039/b009711j. 
  7. ↑ Fox, B. A.; Threlfall, T. L. (1964). "2,3-Diaminopyridine". Organic Syntheses 44: 34. doi:10.15227/orgsyn.044.0034. 
  8. ↑ Mahood, S. A.; Schaffner\doi=10.15227/orgsyn.011.0032, P. V. L. (1931). "2,4-Diaminotoluene". Organic Syntheses 11: 32. doi:10.15227/orgsyn.011.0032. 
  9. ↑ "O-Aminobenzaldehyde, Redox-Neutral Aminal Formation and Synthesis of Deoxyvasicinone". Organic Syntheses 89: 274. 2012. doi:10.15227/orgsyn.089.0274. 
  10. ↑ Redemann, C. T.; Redemann, C. E. (1955). "5-Amino-2,3-dihydro-1,4-phthalazinedione". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv3p0069. ; Collective Volume, 3, pp. 69 
  11. ↑ Hartman, W. W.; Silloway, H. L. (1945). "2-Amino-4-nitrophenol". Organic Syntheses 25: 5. doi:10.15227/orgsyn.025.0005. 
  12. ↑ Faul, Margaret M.; Thiel, Oliver R. (2005). Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rt112.pub2. ISBN 9780470842898. 
  13. ↑ Basu, M. K. (2000). "Ultrasound-promoted highly efficient reduction of aromatic nitro compounds to the aromatic amines by samarium/ammonium chloride". Tetrahedron Lett. 41 (30): 5603–5606. doi:10.1016/S0040-4039(00)00917-5. 
  14. ↑ Kumar, J. S. Dileep; Ho, ManKit M.; Toyokuni, Tatsushi (2001). "Simple and chemoselective reduction of aromatic nitro compounds to aromatic amines: reduction with hydriodic acid revisited". Tetrahedron Letters 42 (33): 5601–5603. doi:10.1016/s0040-4039(01)01083-8. 
  15. ↑ Ayyangar, N. R.; Brahme, K. C.; Kalkote, U. R.; Srinivasan, K. V. (1984). "Facile Transfer-Reduction of Nitroarenes to N Arylhydroxylamines with Hydrazine in the Presence of Raney Nickel". Synthesis 1984 (11): 938. doi:10.1055/s-1984-31027. 
  16. ↑ Harman, R. E. (1963). "Chloro-p-benzoquinone". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv4p0148. ; Collective Volume, 4, pp. 148 
  17. ↑ Kamm, O. (1941). "β-Phenylhydroxylamine". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv1p0445. ; Collective Volume, 1, pp. 445 
  18. ↑ Ichikawa, S.; Zhu, S.; Buchwald, S. (2018). "A Modified System for the Synthesis of Enantioenriched N-Arylamines through Copper-Catalyzed Hydroamination". Angewandte Chemie International Edition 57 (28): 8714–8718. doi:10.1002/anie.201803026. PMID 29847002. 
  19. ↑ 19.0 19.1 Bigelow, H. E.; Robinson, D. B. (1955). "Azobenzene". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv3p0103. ; Collective Volume, 3, pp. 103 
  20. ↑ R. F. Nystrom; W. G. Brown (1948). "Reduction of Organic Compounds by Lithium Aluminum Hydride. III. Halides, Quinones, Miscellaneous Nitrogen Compounds". J. Am. Chem. Soc. 70 (11): 3738–3740. doi:10.1021/ja01191a057. PMID 18102934. 
  21. ↑ M. J. Guttieri; W. F. Maier (1984). "Selective cleavage of carbon-nitrogen bonds with platinum". J. Org. Chem. 49 (16): 2875–2880. doi:10.1021/jo00190a006. 
  22. ↑ T. V. (Babu) RajanBabu, Philip C. Bulman Page, Benjamin R. Buckley, "Tri-n-butylstannane" Encyclopedia of Reagents for Organic Synthesis 2004, John Wiley & Sons. doi:10.1002/047084289X.rt181.pub2
  23. ↑ A. T. Nielsen (1962). "The Isomeric Dinitrocyclohexanes. II. Stereochemistry". J. Org. Chem. 27 (6): 1998–2001. doi:10.1021/jo01053a019. 
  24. ↑ Dauben, Jr., H. J.; Ringold, H. J.; Wade, R. H.; Pearson, D. L.; Anderson, Jr., A. G. (1963). "Cycloheptanone". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv4p0221. ; Collective Volume, 4, pp. 221 
  25. ↑ Senkus, M. (1948). "Iron Reduction of Some Aliphatic Nitro Compounds". Ind. Eng. Chem. 40: 506. doi:10.1021/ie50459a035. 
  26. ↑ A. S. Kende; J. S. Mendoza (1991). "Controlled reduction of nitroalkanes to alkyl hydroxylamines or amines by samarium diiodide". Tetrahedron Letters 32 (14): 1699–1702. doi:10.1016/S0040-4039(00)74307-3. 
  27. ↑ A. Burger, M. L. Stein and J. B. Clements (1957). "Some Pyridylnitroalkenes, Nitroalkanols, and Alkylamines". J. Org. Chem. 22 (2): 143–144. doi:10.1021/jo01353a010. 
  28. ↑ Giannis, A.; Sandhoff, K. (1989). "LiBH4(NaBH4)/Me3SiCl, an Unusually Strong and Versatile Reducing Agent" (in en). Angewandte Chemie International Edition in English 28 (2): 218–220. doi:10.1002/anie.198902181. 
  29. ↑ Butterick, John R.; Unrau, A. M. (1974). "Reduction of β-nitrostyrene with sodium bis-(2-methoxyethoxy)-aluminium dihydride. A convenient route to substituted phenylisopropylamines" (in en). J. Chem. Soc., Chem. Commun. (8): 307–308. doi:10.1039/c39740000307. 
  30. ↑ H. Feuer, R. S. Bartlett, B. F. Vincent and R. S. Anderson (1965). "Diborane Reduction of Nitro Salts. A New Synthesis of N-Monosubstituted Hydroxylamines". J. Org. Chem. 30 (9): 2880–2882. doi:10.1021/jo01020a002. 
  31. ↑ Smith, P.W.G.; Tatchell, A.R. (1965), "Aliphatic Nitro Compounds and Amines" (in en), Fundamental Aliphatic Chemistry (Elsevier): pp. 245–266, doi:10.1016/b978-0-08-010746-2.50016-8, ISBN 978-0-08-010746-2, https://linkinghub.elsevier.com/retrieve/pii/B9780080107462500168, retrieved 2021-01-27 
  32. ↑ Kelly, Sean M.; Lipshutz, Bruce H. (2014-01-03). "Chemoselective Reductions of Nitroaromatics in Water at Room Temperature" (in en). Organic Letters 16 (1): 98–101. doi:10.1021/ol403079x. ISSN 1523-7060. PMID 24341483. 
  33. ↑ Ung, Stéphane; Falguières, Annie; Guy, Alain; Ferroud, Clotilde (August 2005). "Ultrasonically activated reduction of substituted nitrobenzenes to corresponding N-arylhydroxylamines" (in en). Tetrahedron Letters 46 (35): 5913–5917. doi:10.1016/j.tetlet.2005.06.126. https://linkinghub.elsevier.com/retrieve/pii/S0040403905014103. 
  34. ↑ Braun, V. J.; Sobecki, W. (1911). "Über primäre Dinitro-, Nitronitrit- und Dialdoxim-Verbindungen der Fettreihe". Chemische Berichte 44 (3): 2526–2534. doi:10.1002/cber.19110440377. https://zenodo.org/record/1426463. 
  35. ↑ J. R. Hanson; E. Premuzic (1967). "Applications of chromous chloride--II : The reduction of some steroidal nitro-compounds". Tetrahedron 23 (10): 4105–4110. doi:10.1016/S0040-4020(01)97921-9. 
  36. ↑ C. Grundmann (1950). "Über die partielle Reduktion von Nitro-cyclohexan". Angewandte Chemie 62 (23–24): 558–560. doi:10.1002/ange.19500622304. Bibcode: 1950AngCh..62..558G. 



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