Kolbe electrolysis


The Kolbe electrolysis or Kolbe reaction is an organic reaction named after Hermann Kolbe. The Kolbe reaction is formally a decarboxylative dimerisation of two carboxylic acids (or carboxylate ions). The overall reaction is:

Mechanism and side-reactions

The reaction mechanism involves a two-stage radical process: electrochemical oxidation first gives an alkylcarboxyl radical, which decarboxylates almost immediately to give an alkyl radical intermediate. The alkyl radicals which combine to form a covalent bond. As an example, electrolysis of acetic acid yields ethane and carbon dioxide:

CH3COOH → CH3COO− → CH3COO· → CH3· + CO2
2CH3· → CH3CH3

Another example is the synthesis of 2,7-dimethyl-2,7-dinitrooctane from 4-methyl-4-nitrovaleric acid:

Kolbe electrolysis, synthesis of 2,7-Dimethyl-2,7-dinitrooctane

Other compounds can trap the radicals formed by decarboxylation, and the Kolbe reaction has also been occasionally used in cross-coupling reactions. If a mixture of two different carboxylates are used, the radical cross-coupling reaction generally gives all combinations of them:

R1COO− + R2COO− → R1−R1 and/or R1−R2 and/or R2−R2

The reaction process can be enhanced and the Hofer–Moest reaction alternative suppressed, by performing the reaction under weakly acidic conditions in protic solvents, and using a high current density and a platinum anodic electrode.

In 2022, it was discovered that the Kolbe electrolysis is enhanced if an alternating square wave current is used instead of a direct current.

Hofer–Moest reaction

In the Hofer–Moest reaction, the alkyl radical undergo further oxidation to form a carbocation, rather than coupling with another alkyl radical, which then reacts with an available nucleophile. The Hofer–Moest reaction, rather than Kolbe radical-coupling, always occurs if the carboxylic acid bears a carbocation-stabilizing side-substituent at the α position, but only sometimes otherwise.

Applications

Kolbe electrolysis has a few industrial applications. The reaction typically yields <50%.

In one example, sebacic acid has been produced commercially by Kolbe electrolysis of adipic acid.

Kolbe electrolysis has been examined for converting biomass into biodiesel and for grafting of carbon electrodes.

See also

References

  1. ↑ Utley, James (1997). "Trends in Organic Electrosynthesis". Chemical Society Reviews. 26 (3): 157. doi:10.1039/cs9972600157.
  2. ↑ Vijh, A. K.; Conway, B. E. (1967). "Electrode Kinetic Aspects of the Kolbe Reaction". Chem Rev. 67 (6): 623–664. doi:10.1021/cr60250a003.
  3. ↑ Sharkey, W. H.; Langkammerer, C. M. (1973). "2,7-Dimethyl-2,7-dinitrooctane". Organic Syntheses; Collected Volumes, vol. 5, p. 445.
  4. 1 2 3 4 Bohn, Martin A.; Paul, Anna; Hilt, Gerhard (15 March 2012). "Electrochemically initiated radical reactions". Encyclopedia of Radicals in Chemistry, Biology and Materials. Vol. Synthetic Strategies and Applications. Wiley. § 2.7. doi:10.1002/9781119953678.rad034. ISBN 978-0-470-97125-3.
  5. ↑ Hioki, Yuta; Costantini, Matteo; Griffin, Jeremy; Harper, Kaid; Prado Merini, Melania; Nissl, Benedikt; Kawamata, Yu; Baran, Phil (31 October 2022). Overcoming the Limitations of Kolbe Coupling via Waveform-Controlled Electrosynthesis (Report). Chemistry. doi:10.26434/chemrxiv-2022-3cj82-v2.
  6. ↑ Hioki, Yuta; Costantini, Matteo; Griffin, Jeremy; Harper, Kaid C.; Merini, Melania Prado; Nissl, Benedikt; Kawamata, Yu; Baran, Phil S. (7 April 2023). "Overcoming the limitations of Kolbe coupling with waveform-controlled electrosynthesis". Science. 380 (6640): 81–87. Bibcode:2023Sci...380...81H. doi:10.1126/science.adf4762. ISSN 0036-8075. PMID 37023204.
  7. ↑ "Hofer–Moest Reaction". Comprehensive Organic Name Reactions and Reagents. 2010. pp. 1443–1446. doi:10.1002/9780470638859.conrr322. ISBN 978-0-471-70450-8.
  8. ↑ Wendt, Hartmut; Vogt, Helmut; Kreysa, Gerhard; m. Kolb, Dieter; e. Engelmann, Gerald; Ziegler, Jörg C.; Goldacker, Hubert; Jüttner, Klaus; Galla, Ulrich; Schmieder, Helmut; Steckhan, Eberhard (2009). "Electrochemistry". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a09_183.pub3. ISBN 978-3-527-30673-2.
  9. ↑ Seko, Maomi; Yomiyama, Akira; Isoya, Toshiro (1979). "Development of Kolbe Electrosynthesis of Sebacic Acid". CEER, Chemical Economy & Engineering Review. 11 (9): 48–50.
  10. ↑ Yuan, Gang; Wu, Chan; Zeng, Guorong; Niu, Xiaopo; Shen, Guoqiang; Wang, Li; Zhang, Xiangwen; Luque, Rafael; Wang, Qingfa (18 January 2020). "Kolbe Electrolysis of Biomass-Derived Fatty Acids Over Pt Nanocrystals in an Electrochemical Cell". ChemCatChem. 12 (2): 642–648. doi:10.1002/cctc.201901443. ISSN 1867-3880.
  11. ↑ Ho, Calvin K.; McAuley, Kimberley B.; Peppley, Brant A. (1 October 2019). "Biolubricants through renewable hydrocarbons: A perspective for new opportunities". Renewable and Sustainable Energy Reviews. 113 109261. doi:10.1016/j.rser.2019.109261. ISSN 1364-0321.
  12. ↑ Andrieux, Claude P.; Gonzalez, Felipe; Savéant, Jean-Michel (1 May 1997). "Derivatization of Carbon Surfaces by Anodic Oxidation of Arylacetates. Electrochemical Manipulation of the Grafted Films". Journal of the American Chemical Society. 119 (18): 4292–4300. doi:10.1021/ja9636092. ISSN 0002-7863.
  13. ↑ Bélanger, Daniel; Pinson, Jean (20 June 2011). "Electrografting: a powerful method for surface modification". Chemical Society Reviews. 40 (7): 3995–4048. doi:10.1039/C0CS00149J. ISSN 1460-4744. PMID 21503288.

Further reading