Claisen condensation
| Claisen condensation | |||||||||||||
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| Named after | Rainer Ludwig Claisen | ||||||||||||
| Reaction type | Condensation reaction | ||||||||||||
| Reaction | |||||||||||||
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| Typical solvents | R'-OH | ||||||||||||
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| Organic Chemistry Portal | claisen-condensation | ||||||||||||
| RSC ontology ID | RXNO:0000043 | ||||||||||||
The Claisen condensation 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. The reaction produces a β-keto ester or a β-diketone. It is named after Rainer Ludwig Claisen, who first published his work on the reaction in 1887. The reaction has often been displaced by diketene-based chemistry, which affords acetoacetic esters.