Claisen condensation

Claisen condensation
Named after Rainer Ludwig Claisen
Reaction type Coupling reaction
Identifiers
Organic Chemistry Portal claisen-condensation
RSC ontology ID RXNO:0000043

The Claisen condensation (not to be confused with the Claisen rearrangement) is a carbon–carbon bond forming reaction that occurs between two esters or one ester and another carbonyl compound in the presence of a strong base, resulting in a β-keto ester or a β-diketone.[1] It is named after Rainer Ludwig Claisen, who first published his work on the reaction in 1887.[2][3][4]

Requirements

At least one of the reagents must be enolizable (have an α-proton and be able to undergo deprotonation to form the enolate anion). There are a number of different combinations of enolizable and nonenolizable carbonyl compounds that form a few different types of Claisen condensations.

The base used must not interfere with the reaction by undergoing nucleophilic substitution or addition with a carbonyl carbon. For this reason, the conjugate sodium alkoxide base of the alcohol formed (e.g. sodium ethoxide if ethanol is formed) is often used, since the alkoxide is regenerated. In mixed Claisen condensations, a non-nucleophilic base such as lithium diisopropylamide, or LDA, may be used, since only one compound is enolizable. LDA is not commonly used in the classic Claisen or Dieckmann condensations due to enolization of the electrophilic ester.

The alkoxy portion of the ester must be a relatively good leaving group. Methyl and ethyl esters, which yields methoxide and ethoxide, respectively, are commonly used.

Types

Mechanism

In the first step of the mechanism, an α-proton is removed by a strong base, resulting in the formation of an enolate anion, which is made relatively stable by the delocalization of electrons. Next, the carbonyl carbon of the (other) ester is nucleophilically attacked by the enolate anion. The alkoxy group is then eliminated (resulting in (re)generation of the alkoxide), and the alkoxide removes the newly formed doubly α-proton to form a new, highly resonance-stabilized enolate anion. Aqueous acid (e.g. sulfuric acid or phosphoric acid) is added in the final step to neutralize the enolate and any base still present. The newly formed β-keto ester or β-diketone is then isolated. Note that the reaction requires a stoichiometric amount of base as the removal of the doubly α-proton thermodynamically drives the otherwise endergonic reaction. That is, Claisen condensation does not work with substrates having only one α-hydrogen because of the driving force effect of deprotonation of the β-keto ester in the last step.

animation

Stobbe condensation

The Stobbe condensation [5] is a modification specific for the diethyl ester of succinic acid requiring less strong bases.[6] An example is its reaction with benzophenone:[7]

A reaction mechanism that explains the formation of both an ester group and a carboxylic acid group is centered on a lactone intermediate (5):

See also

References

  1. Carey, F. A. (2006). Organic Chemistry (6th ed.). New York, NY: McGraw-Hill. ISBN 0-07-111562-5.
  2. Claisen, L.; Claparede, A. (1881). "Condensationen von Ketonen mit Aldehyden". Berichte der Deutschen Chemischen Gesellschaft 14 (2): 2460–2468. doi:10.1002/cber.188101402192.
  3. Claisen, L. (1887). "Ueber die Einführung von Säureradicalen in Ketone". Berichte der Deutschen Chemischen Gesellschaft 20 (1): 655–657. doi:10.1002/cber.188702001150.
  4. Hauser, C. R.; Hudson, B. E. Jr. (1942). "The Acetoacetic Ester Condensation and Certain Related Reactions". Organic Reactions 1. doi:10.1002/0471264180.or001.09.
  5. Stobbe, H. (1899). "Condensation des Benzophenons mit Bernsteinsäureester". Justus Liebigs Annalen der Chemie 308 (1–2): 89–114. doi:10.1002/jlac.18993080106.
  6. March, Jerry (1985), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (3rd ed.), New York: Wiley, ISBN 0-471-85472-7
  7. Johnson, W. S.; Schneider, W. P. (1950). "β-CARBETHOXY-γ,γ-DIPHENYLVINYLACETIC ACID" (PDF). Org. Synth. 30: 18.; Coll. Vol. 4, p. 132

External links

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