Tishchenko reaction

The Tishchenko reaction is an organic chemical reaction that involves disproportionation of an aldehyde in the presence of an alkoxide. The reaction is named after Russian organic chemist Vyacheslav Tishchenko, who discovered that aluminium alkoxides are effective catalysts for the reaction.[1][2] [3]

Tishchenko reaction
Named after Vyacheslav Tishchenko
Reaction type Organic redox reaction
Identifiers
Organic Chemistry Portal tishchenko-reaction

In the related Cannizzaro reaction, the base is sodium hydroxide and then the oxidation product is a carboxylic acid and the reduction product is an alcohol.

History

The reaction involving benzaldehyde was discovered by Claisen using sodium benzylate as base.[1] The reaction produces benzyl benzoate.[4]

Enolizable aldehydes are not amenable to Claisen's conditions. Vyacheslav Tishchenko discovered that aluminium alkoxides allowed the conversion of enolizable aldehydes to esters.

Examples
  • The Tishchenko reaction of acetaldehyde gives the commercially important solvent ethyl acetate. The reaction is catalyzed by aluminium alkoxides.[5]
  • The Tishchenko reaction is used to obtain isobutyl isobutyrate, a specialty solvent.[6]
  • Hydroxypivalic acid neopentyl glycol ester is produced by a Tishchenko reaction from hydroxypivaldehyde in the presence of a basic catalyst (e.g., aluminium oxide).[7]
  • The Tishchenko reaction of paraformaldehyde in the presence of aluminum methylate or magnesium methylate forms methyl formate.[8]
  • Paraformaldehyde reacts with boric acid to form methyl formate.[9] The key step in the reaction mechanism for this reaction is a 1,3-hydride shift in the hemiacetal intermediate formed from two successive nucleophilic addition reactions, the first one from the catalyst. The hydride shift regenerates the alkoxide catalyst.

See also

References
  1. Seki, Tsunetake; Nakajo, Tetsuo; Onaka, Makoto (2006). "The Tishchenko Reaction: A Classic and Practical Tool for Ester Synthesis". Chemistry Letters. 35 (8): 824–829. doi:10.1246/cl.2006.824.
  2. Mlynarski, Jacek (2006). "Direct Asymmetric Aldol-Tishchenko Reaction". European Journal of Organic Chemistry. 2006 (21): 4779–4786. doi:10.1002/ejoc.200600258.
  3. Hattori, Hideshi (2001). "Solid base catalysts: Generation of basic sites and application to organic synthesis". Applied Catalysis A: General. 222 (1–2): 247–259. doi:10.1016/S0926-860X(01)00839-0.
  4. Kamm, O.; Kamm, W. F. (1922). "Benzyl benzoate". Organic Syntheses. 2: 5. doi:10.15227/orgsyn.002.0005.
  5. Eckert, Marc; Fleischmann, Gerald; Jira, Reinhard; Bolt, Hermann M.; Golka, Klaus (15 December 2006). "Acetaldehyde". Ullmann's Encyclopedia of Industrial Chemistry. Wiley. doi:10.1002/14356007.a01_031.pub2. ISBN 3527306730.
  6. Cornils, Boy; Fischer, Richard W.; Kohlpaintner, Christian (15 September 2000). "Butanals". Ullmann's Encyclopedia of Industrial Chemistry. Wiley. doi:10.1002/14356007.a04_447. ISBN 3527306730.
  7. Werle, Peter; Morawietz, Marcus (15 June 2000). "Alcohols, Polyhydric". Ullmann's Encyclopedia of Industrial Chemistry. Wiley. doi:10.1002/14356007.a01_305. ISBN 3527306730.
  8. Reuss, Günther; Disteldorf, Walter; Gamer, Armin Otto; Hilt, Albrecht (15 June 2000). "Formaldehyde". Ullmann's Encyclopedia of Industrial Chemistry. Wiley. doi:10.1002/14356007.a11_619. ISBN 3527306730.
  9. Paul R. Stapp (1973). "Boric acid catalyzed Tishchenko reactions". Journal of Organic Chemistry. 38 (7): 1433–1434. doi:10.1021/jo00947a049.

Further reading
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