Nitration

Not to be confused with Nitrification.

Nitration is a general class of chemical process for the introduction of a nitro group into an organic chemical compound. More loosely the term also is applied incorrectly to the different process of forming nitrate esters between alcohols and nitric acid, as occurs in the synthesis of nitroglycerin. The difference between the resulting structure of nitro compounds and nitrates is that the nitrogen atom in nitro compounds is directly bonded to a non-oxygen atom, typically carbon or another nitrogen atom, whereas in nitrate esters, also called organic nitrates, the nitrogen is bonded to an oxygen atom that in turn usually is bonded to a carbon atom.

There are many major industrial applications of nitration in the strict sense; the most important by volume are for the production of Nitroaromatic compounds such as nitrobenzene. Nitration reactions are notably used for the production of explosives, for example the conversion of guanidine to nitroguanidine and the conversion of toluene to trinitrotoluene. However, they are of wide importance as chemical intermediates and precursors. Millions of tons of nitroaromatics are produced annually.[1]

Aromatic nitration

Typical nitration syntheses apply so-called "mixed acid", a mixture of concentrated nitric acid and sulfuric acids.[2] This mixture produces the nitronium ion (NO2+), which is the active species in aromatic nitration. This active ingredient, which can be isolated in the case of nitronium tetrafluoroborate,[3] also effects nitration without the need for the mixed acid. In mixed-acid syntheses sulfuric acid is not consumed and hence acts as a catalyst as well as an absorbent for water. In the case of nitration of benzene, the reaction is conducted at 50 °C. The process is one example of electrophilic aromatic substitution, which involves the attack by the electron-rich benzene ring:

Alternative mechanisms have also been proposed, including one involving single electron transfer (SET).[4][5]

Scope

Selectivity can be a challenge in nitrations because as a rule more than one compound may result but only one is desired, so alternative products act as contaminants or are simply wasted. Accordingly, it is desirable to design syntheses with suitable selectivity; for example, by controlling the reaction conditions, fluorenone can be selectively trinitrated[6] or tetranitrated.[7]


The substituents on aromatic rings affect the rate of this electrophilic aromatic substitution. Deactivating groups such as other nitro groups have an electron-withdrawing effect. Such groups deactivate (slow) the reaction and directs the electrophilic nitronium ion to attack the aromatic meta position. Deactivating meta-directing substituents include sulfonyl, cyano groups, keto, esters, and carboxylates. Nitration can be accelerated by activating groups such as amino, hydroxy and methyl groups also amides and ethers resulting in para and ortho isomers.

The direct nitration of aniline with nitric acid and sulfuric acid, according to one source [8] results in a 50/50 mixture of para and meta nitroaniline. In this reaction the fast-reacting and activating aniline (ArNH2) exists in equilibrium with the more abundant but less reactive (deactivated) anilinium ion (ArNH3+), which may explain this reaction product distribution. According to another source [9] a more controlled nitration of aniline starts with the formation of acetanilide by reaction with acetic anhydride followed by the actual nitration. Because the amide is a regular activating group the products formed are the para and ortho isomers. Heating the reaction mixture is sufficient to hydrolyze the amide back to the nitrated aniline.

In the Wolfenstein-Boters reaction, benzene reacts with nitric acid and mercury nitrate to give picric acid.

Ipso nitration

With aryl chlorides, triflates and nonaflates ipso substitution can take place as well in so-called ipso nitration.[10] The phrase was first used by Perrin and Skinner in 1971 in an investigation into chloroanisole nitration [11] In one protocol 4-chloro-n-butylbenzene is reacted with sodium nitrite in t-butanol in presence of 0.5 mol% Pd2(dba)3, a biarylphosphine ligand and a phase-transfer catalyst to 4-nitro-n-butylbenzene [12]

References

  1. ↑ Gerald Booth "Nitro Compounds, Aromatic" Ullmann's Encyclopedia of Industrial Chemistry, 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a17_411
  2. ↑ John McMurry Organic Chemistry 2nd Ed.
  3. ↑ George A. Olah and Stephen J. Kuhn. "Benzonitrile, 2-methyl-3,5-dinitro-". Org. Synth.; Coll. Vol. 5, p. 480
  4. ↑ Esteves, P. M.; Carneiro, J. W. M.; Cardoso, S. P.; Barbosa, A. G. H.; Laali, K. K.; Rasul, G.; Prakash, G. K. S.; e Olah, G. A. (2003). "Unified Mechanism Concept of Electrophilic Aromatic Nitration Revisited: Convergence of Computational Results and Experimental Data". J. Am. Chem. Soc. 125 (16): 4836–49. doi:10.1021/ja021307w. PMID 12696903.
  5. ↑ Queiroz, J. F.; Carneiro, J. W. M.; Sabino A. A.; Sparapan, R.; Eberlin, M. N.; Esteves, P. M. (2006). "Electrophilic Aromatic Nitration: Understanding Its Mechanism and Substituent Effects". J. Org. Chem. 71 (16): 6192–203. doi:10.1021/jo0609475. PMID 16872205.
  6. ↑ E. O. Woolfolk and Milton Orchin. "2,4,7-Trinitrofluorenone". Org. Synth.; Coll. Vol. 3, p. 837
  7. ↑ Melvin S. Newman and H. Boden. "2,4,5,7-Tetranitrofluorenone". Org. Synth.; Coll. Vol. 5, p. 1029
  8. ↑ Web resource: warren-wilson.edu
  9. ↑ Mechanism and synthesis Peter Taylor,Royal Society of Chemistry (Great Britain),Open University
  10. ↑ Prakash, G.; Mathew, T. (2010). "Ipso-Nitration of Arenes". Angewandte Chemie International Edition in English 49 (10): 1726–1728. doi:10.1002/anie.200906940. PMID 20146295.
  11. ↑ Perrin, C. L.; Skinner, G. A. (1971). "Directive effects in electrophilic aromatic substitution ("ipso factors"). Nitration of haloanisoles". Journal of the American Chemical Society 93 (14): 3389. doi:10.1021/ja00743a015.
  12. ↑ Fors, B.; Buchwald, S. (2009). "The Pd-Catalyzed Conversion of Aryl Chlorides, Triflates, and Nonaflates to Nitroaromatics". Journal of the American Chemical Society 131 (36): 12898–12899. doi:10.1021/ja905768k. PMC 2773681. PMID 19737014.
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