Tishchenko reaction explained
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]
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
See also
Further reading
- V. E. . Tishchenko . О действии алкоголятов алюминия на альдегиды. Сложного-эфира конденсации, как новый вид уплотнения альдегида. . On the effect of aluminium alkoxides on aldehydes. Ester condeNsation, as a new kind of aldehyde condensation. . Журнал Русского Физико-Химического Общества (Journal of the Russian Physico-Chemical Society) . 38 . 1906 . 355–418 . ; 482–540. (in Russian)
- В. Е. Тищенко and Г. Н. Григорьева (V. E. Tishchenko and G. N. Grigor'eva) (1906) "О действии амальгамы магния на изомасляного альдегида" (On the effect of magnesium amalgam on isobutyric aldehyde), Журнал Русского Физико-Химического Общества (Journal of the Russian Physico-Chemical Society), 38 : 540–547. (in Russian)
- М. П. Воронҝова and В. Е. Тищенко (M. P. Voronkova and V. E. Tishchenko) (1906) "О действии амальгамы магния на уксусный альдегид" (On the effect of magnesium amalgam on acetic aldehyde), Журнал Русского Физико-Химического Общества (Journal of the Russian Physico-Chemical Society), 38 : 547–550. (in Russian)
- В. Тищенко (V. Tishchenko) (1899) "Действие амальгамированного алюминия на алкоголь. Алкоголятов алюминия, их свойства и реакции." (Effect of amalgamated aluminium on alcohol. Aluminium alkoxides, their properties and reactions.), Журнал Русского Физико-Химического Общества (Journal of the Russian Physico-Chemical Society), 31 : 694–770. (in Russian)
Notes and References
- 10.1246/cl.2006.824. The Tishchenko Reaction: A Classic and Practical Tool for Ester Synthesis. Chemistry Letters. 35. 8. 824–829. 2006. Seki. Tsunetake. Nakajo. Tetsuo. Onaka. Makoto.
- 10.1002/ejoc.200600258. Direct Asymmetric Aldol-Tishchenko Reaction. European Journal of Organic Chemistry. 2006. 21. 4779–4786. 2006. Mlynarski. Jacek.
- 10.1016/S0926-860X(01)00839-0. Solid base catalysts: Generation of basic sites and application to organic synthesis. Applied Catalysis A: General. 222. 1–2. 247–259. 2001. Hattori. Hideshi.
- Kamm . O. . Kamm . W. F. . Benzyl benzoate . Organic Syntheses . 1922 . 2 . 5 . 10.15227/orgsyn.002.0005 .
- Encyclopedia: Marc . Eckert . Gerald . Fleischmann . Reinhard . Jira . Hermann M. . Bolt . Klaus . Golka . Acetaldehyde . . 10.1002/14356007.a01_031.pub2 . Wiley . 15 December 2006. 3527306730 .
- Encyclopedia: Boy . Cornils . Richard W. . Fischer . Christian . Kohlpaintner . Butanals . . Wiley . 15 September 2000 . 10.1002/14356007.a04_447. 3527306730 .
- Encyclopedia: Peter . Werle . Marcus . Morawietz . Alcohols, Polyhydric . . Wiley . 15 June 2000 . 10.1002/14356007.a01_305. 3527306730 .
- Encyclopedia: Günther . Reuss . Walter . Disteldorf . Armin Otto . Gamer . Albrecht . Hilt . Formaldehyde . . Wiley . 15 June 2000 . 10.1002/14356007.a11_619. 3527306730 .
- Paul R. Stapp . . 1973 . 38 . 7 . 1433–1434 . 10.1021/jo00947a049 . Boric acid catalyzed Tishchenko reactions.