Nitro compound explained

See also: Transition metal nitrite complex.

In organic chemistry, nitro compounds are organic compounds that contain one or more nitro functional groups . The nitro group is one of the most common explosophores (functional group that makes a compound explosive) used globally. The nitro group is also strongly electron-withdrawing. Because of this property, bonds alpha (adjacent) to the nitro group can be acidic. For similar reasons, the presence of nitro groups in aromatic compounds retards electrophilic aromatic substitution but facilitates nucleophilic aromatic substitution. Nitro groups are rarely found in nature. They are almost invariably produced by nitration reactions starting with nitric acid.^[1]

Synthesis

Preparation of aromatic nitro compounds

Aromatic nitro compounds are typically synthesized by nitration. Nitration is achieved using a mixture of nitric acid and sulfuric acid, which produce the nitronium ion, which is the electrophile:

+

The nitration product produced on the largest scale, by far, is nitrobenzene. Many explosives are produced by nitration including trinitrophenol (picric acid), trinitrotoluene (TNT), and trinitroresorcinol (styphnic acid).Another but more specialized method for making aryl–NO₂ group starts from halogenated phenols, is the Zinke nitration.

Preparation of aliphatic nitro compounds

Aliphatic nitro compounds can be synthesized by various methods; notable examples include:

• Free radical nitration of alkanes.^[2] The reaction produces fragments from the parent alkane, creating a diverse mixture of products; for instance, nitromethane, nitroethane, 1-nitropropane, and 2-nitropropane are produced by treating propane with nitric acid in the gas phase (e.g. 350–450 °C and 8–12 atm).
• Nucleophilic substitution reactions between halocarbons^[3] or organosulfates^[4] with silver or alkali nitrite salts.
• Nitromethane can be produced in the laboratory by treating sodium chloroacetate with sodium nitrite.^[5]
• Oxidation of oximes^[6] or primary amines.^[7]
• Reduction of β-nitro alcohols^[8] or nitroalkenes.^[9]
• By decarboxylation of α-nitro carboxylic acids formed from nitriles and ethyl nitrate.^{[10] [11]}

Ter Meer Reaction

In nucleophilic aliphatic substitution, sodium nitrite (NaNO₂) replaces an alkyl halide. In the so-called Ter Meer reaction (1876) named after Edmund ter Meer,^[12] the reactant is a 1,1-halonitroalkane:

The reaction mechanism is proposed in which in the first slow step a proton is abstracted from nitroalkane 1 to a carbanion 2 followed by protonation to an aci-nitro 3 and finally nucleophilic displacement of chlorine based on an experimentally observed hydrogen kinetic isotope effect of 3.3.^[13] When the same reactant is reacted with potassium hydroxide the reaction product is the 1,2-dinitro dimer.^[14]

Occurrence

In nature

Chloramphenicol is a rare example of a naturally occurring nitro compound. At least some naturally occurring nitro groups arose by the oxidation of amino groups.^[15] 2-Nitrophenol is an aggregation pheromone of ticks.

Examples of nitro compounds are rare in nature. 3-Nitropropionic acid found in fungi and plants (Indigofera). Nitropentadecene is a defense compound found in termites. Aristolochic acids are found in the flowering plant family Aristolochiaceae. Nitrophenylethane is found in Aniba canelilla.^[16] Nitrophenylethane is also found in members of the Annonaceae, Lauraceae and Papaveraceae.^[17]

In pharmaceuticals

Despite the occasional use in pharmaceuticals, the nitro group is associated with mutagenicity and genotoxicity and therefore is often regarded as a liability in the drug discovery process.^[18]

Reactions

Nitro compounds participate in several organic reactions, the most important being reduction of nitro compounds to the corresponding amines:

RNO₂ + 3 H₂ → RNH₂ + 2 H₂OVirtually all aromatic amines (e.g. aniline) are derived from nitroaromatics through such catalytic hydrogenation. A variation is formation of a dimethylaminoarene with palladium on carbon and formaldehyde:^[19]

The α-carbon of nitroalkanes is somewhat acidic. The pK_a values of nitromethane and 2-nitropropane are respectively 17.2 and 16.9 in dimethyl sulfoxide (DMSO) solution, suggesting an aqueous pK_a of around 11.^[20] In other words, these carbon acids can be deprotonated in aqueous solution. The conjugate base is called a nitronate, and behaves similar to an enolate. In the nitroaldol reaction, it adds directly to aldehydes, and, with enones, can serve as a Michael donor. Conversely, a nitroalkene reacts with enols as a Michael acceptor.^{[21] [22]}

Nitronates are also key intermediates in the Nef reaction: when exposed to acids or oxidants, a nitronate hydrolyzes to a carbonyl and azanone.^[23]

Grignard reagents combine with nitro compounds to give a nitrone; but a Grignard reagent with an α hydrogen will then add again to the nitrone to give a hydroxylamine salt.^[24]

Dye syntheses

The Leimgruber–Batcho, Bartoli and Baeyer–Emmerling indole syntheses begin with aromatic nitro compounds. Indigo can be synthesized in a condensation reaction from ortho-nitrobenzaldehyde and acetone in strongly basic conditions in a reaction known as the Baeyer–Drewson indigo synthesis.

Biochemical reactions

Many flavin-dependent enzymes are capable of oxidizing aliphatic nitro compounds to less-toxic aldehydes and ketones. Nitroalkane oxidase and 3-nitropropionate oxidase oxidize aliphatic nitro compounds exclusively, whereas other enzymes such as glucose oxidase have other physiological substrates.^[25]

Explosions

Explosive decomposition of organo nitro compounds are redox reactions, wherein both the oxidant (nitro group) and the fuel (hydrocarbon substituent) are bound within the same molecule. The explosion process generates heat by forming highly stable products including molecular nitrogen (N₂), carbon dioxide, and water. The explosive power of this redox reaction is enhanced because these stable products are gases at mild temperatures. Many contact explosives contain the nitro group.

See also

• Functional group
• Reduction of nitro compounds
• Nitration
• Nitrite (also an NO₂ group, but bonds differently)
• Nitroalkene
• Nitroglycerin

Notes and References

1. Book: Nitro and Nitroso Groups: Part 2, Volume 2 . 1970 . Henry Feuer . 978-0-470-77117-4 . 10.1002/9780470771174 . John Wiley & Sons Ltd. . PATAI'S Chemistry of Functional Groups. 2 . Book: Nitro and Nitroso Groups: Supplement F: Part 2, Volume 2 . 1982 . Saul Patai . 978-0-470-77167-9 . 10.1002/9780470771679 . John Wiley & Sons Ltd. . PATAI'S Chemistry of Functional Groups. Book: Amino, Nitroso and Nitro Compounds and Their Derivatives: Supplement F: Part 1, Volume 1 . 1982 . Saul Patai . 978-0-470-77166-2 . 10.1002/9780470771662 . John Wiley & Sons Ltd. . PATAI'S Chemistry of Functional Groups.
2. Markofsky. Sheldon. Grace. W.G.. Nitro Compounds, Aliphatic. Ullmann's Encyclopedia of Industrial Chemistry. 2000. 10.1002/14356007.a17_401. 978-3-527-30673-2.
3. Kornblum. N.. Ungnade. H. E.. 1-Nitroöctane. Organic Syntheses. 1963. 4. 724. 10.15227/orgsyn.038.0075.
4. Walden. P.. Zur Darstellung aliphatischer Sulfocyanide, Cyanide und Nitrokörper. Berichte der Deutschen Chemischen Gesellschaft. 1907. 40. 3. 3214–3217. 10.1002/cber.19070400383.
5. Whitmore. F. C.. Whitmore. Marion G.. Nitromethane. Organic Syntheses. 1923. 1. 401. 10.15227/orgsyn.003.0083.
6. Olah. George A.. Ramaiah. Pichika. Chang-Soo. Lee. Prakash. Surya. Convenient Oxidation of Oximes to Nitro Compounds with Sodium Perborate in Glacial Acetic Acid. Synlett. 1992. 1992. 4. 337–339. 10.1055/s-1992-22006.
7. Ehud. Keinan. Yehuda. Mazur. Dry ozonation of amines. Conversion of primary amines to nitro compounds. The Journal of Organic Chemistry. 1977. 42. 5. 844–847. 10.1021/jo00425a017.
8. Chandrasekhar . S. . Shrinidhi . A. . Useful Extensions of the Henry Reaction: Expeditious Routes to Nitroalkanes and Nitroalkenes in Aqueous Media . Synthetic Communications . 2014 . 44 . 20 . 3008–3018 . 10.1080/00397911.2014.926373. 98439096 .
9. Shrinidhi . A. . Microwave-assisted chemoselective reduction of conjugated nitroalkenes to nitroalkanes with aqueous tri-n-butyltin hydride . Cogent Chemistry . 2015 . 1 . 1 . 1061412 . 10.1080/23312009.2015.1061412. free .
10. Wislicenus. Wilhelm. Endres. Anton. Ueber Nitrirung mittels Aethylnitrat [Nitrification by means of ethyl nitrate]]. Berichte der Deutschen Chemischen Gesellschaft. 1902. 35. 2. 1755–1762. 10.1002/cber.190203502106.
11. Book: Weygand. Conrad. Hilgetag. G.. Martini. A.. Weygand/Hilgetag Preparative Organic Chemistry. 1972. John Wiley & Sons, Inc.. New York. 978-0-471-93749-4. 1007. 4th.
12. Edmund ter Meer . Ueber Dinitroverbindungen der Fettreihe . . 181 . 1 . 1–22 . 1876 . 10.1002/jlac.18761810102. Edmund ter Meer .
13. 10.1021/ja01600a048 . Aci-Nitroalkanes. I. The Mechanism of the ter Meer Reaction1 . Journal of the American Chemical Society . 78 . 19 . 4980–4984 . 1956 . Hawthorne . M. Frederick.
14. 3-Hexene, 3,4-dinitro- D. E. Bisgrove, J. F. Brown, Jr., and L. B. Clapp. Organic Syntheses, Coll. Vol. 4, p. 372 (1963); Vol. 37, p. 23 (1957). (Article)
15. 10.1016/j.jmb.2007.06.014 . 17765264 . Structure and Action of the N-oxygenase AurF from Streptomyces thioluteus . Journal of Molecular Biology . 373 . 1 . 65–74 . 2007 . Zocher . Georg . Winkler . Robert . Hertweck . Christian . Schulz . Georg E.
16. Maia . José Guilherme S. . Andrade . Eloísa Helena A. . Database of the Amazon aromatic plants and their essential oils . Química Nova . FapUNIFESP (SciELO) . 32 . 3 . 2009 . 0100-4042 . 10.1590/s0100-40422009000300006 . 595–622 . free .
17. Book: Kramer . K.U. . Kubitzki . K. . Rohwer . J.G. . Bittrich . V. . Flowering Plants, Dicotyledons: Magnoliid, Hamamelid, and Caryophyllid Families . Springer-Verlag, Berlin . Families and genera of vascular plants . 1993 . 978-3-540-55509-4 .
18. Nepali K, Lee HY, Liou JP . Nitro-Group-Containing Drugs . J. Med. Chem. . 62 . 6 . 2851–2893 . March 2019 . 30295477 . 10.1021/acs.jmedchem.8b00147 . 52931949 .
19. ETHYL p-DIMETHYLAMINOPHENYLACETATE . Organic Syntheses. 1967. 47. 69. 10.15227/orgsyn.047.0069.
20. 10.1021/ja00099a004. Is Resonance Important in Determining the Acidities of Weak Acids or the Homolytic Bond Dissociation Enthalpies (BDEs) of Their Acidic H-A Bonds?. Journal of the American Chemical Society. 116. 20. 8885. 1994. Bordwell. Frederick G. Satish. A. V.
21. Ranganathan, Darshan . Rao, Bhushan . Ranganathan, Subramania . Mehrotra, Ashok . Iyengar, Radha . amp . Nitroethylene: a stable, clean, and reactive agent for organic synthesis. The Journal of Organic Chemistry. 1980. 45. 7. 1185–1189. 10.1021/jo01295a003.
22. Jubert, Carole . Knochel, Paul . amp . Preparation of polyfunctional nitro olefins and nitroalkanes using the copper-zinc reagents RCu(CN)ZnI. The Journal of Organic Chemistry. 1992. 57. 20. 5431–5438. 10.1021/jo00046a027.
23. Smith (2020)), March's Organic Chemistry, rxn. 16-3.
24. 10.1021/jo00048a012. Nitrones from addition of benzyl and allyl Grignard reagents to alkyl nitro compounds: chemo-, regio-, and stereoselectivity of the reaction. Giuseppe. Bartoli. Enrico. Marcantoni. Marino. Petrini. 14 Apr 1992. American Chemical Society. Journal of Organic Chemistry. 57. 22. 1992. 5834–5840.
25. Nagpal. Akanksha. Michael P. . Valley . Paul F. . Fitzpatrick . Allen M. . Orville . 2006. Crystal Structures of Nitroalkane Oxidase: Insights into the Reaction Mechanism from a Covalent Complex of the Flavoenzyme Trapped during Turnover. Biochemistry. 16430210. 10.1021/bi051966w. 45. 4. 1855086. 1138–50.