Dieckmann condensation
Topic: Chemistry
From HandWiki - Reading time: 4 min
| Dieckmann condensation | |
|---|---|
| Named after | Walter Dieckmann |
| Reaction type | Ring forming reaction |
| Identifiers | |
| Organic Chemistry Portal | dieckmann-condensation |
| RSC ontology ID | RXNO:0000065 |
The Dieckmann condensation is the intramolecular chemical reaction of diesters with base to give β-keto esters.[1] It is named after the German chemist Walter Dieckmann (1869–1925).[2][3] The equivalent intermolecular reaction is the Claisen condensation. Dieckmann condensations are highly effective routes to 5-, 6-, and 7-member rings, but poor for larger rings.[4]
The Dieckmann condensation
Reaction mechanism
Deprotonation of an ester at the α-position generates an enolate ion which then undergoes a 5-exo-trig nucleophilic attack to give a cyclic enol. Protonation with a Brønsted-Lowry acid (H3O+ for example) re-forms the β-keto ester.[5]
Dieckmann condensation reaction mechanism for the example given
Due to the steric stability of five- and six-membered rings, these structures will preferentially be formed. 1,6 diesters will form five-membered cyclic β-keto esters, while 1,7 diesters will form six-membered β-keto esters.[6]
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| Animation of the reaction mechanism |
Further reading
- Dieckmann, W. Ber. 1894, 27, 102 & 965
- Dieckmann, W. Ber. 1900, 33, 595 & 2670
- Dieckmann, W. Ann. 1901, 317, 51 & 93
See also
References
- ↑ Davis, B. R.; Garrett, P. J. Compr. Org. Synth. 1991, 2, 806-829. (Review)
- ↑ Kwart, Harold; King, Kenneth (1969). "Rearrangement and cyclization reactions of carboxylic acids and esters". in S. Patai. PATAI'S Chemistry of Functional Groups: Carboxylic Acids and Esters (1969). pp. 341–373. doi:10.1002/9780470771099.ch8. ISBN 9780470771099.
- ↑ Schaefer, J. P.; Bloomfield, J. J. (1967). "The Dieckmann Condensation (Including the Thorpe-Ziegler Condensation)". Organic Reactions 15: 1–203. doi:10.1002/0471264180.or015.01. ISBN 0471264180.
- ↑ Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, p. 1453, ISBN 978-0-471-72091-1, https://books.google.com/books?id=JDR-nZpojeEC&printsec=frontcover
- ↑ Janice Gorzynski Smith (2007). Organic Chemistry (2nd ed.). pp. 932–933. ISBN 978-0073327495. https://archive.org/details/organicchemistry00smit_600.
- ↑ "Dieckmann Condensation". Organic Chemistry Portal. https://www.organic-chemistry.org/namedreactions/dieckmann-condensation.shtm.
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