Japp–Klingemann reaction: Difference between revisions
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{{Short description|A chemical reaction used in organic synthesis}} | |||
The '''Japp–Klingemann reaction''' is a chemical reaction used in organic chemistry | The '''Japp–Klingemann reaction''' is a chemical reaction used in organic chemistry to synthesize [[hydrazone]]s from [[aryl diazonium salt]]s and [[_-keto acid]]s or their esters. This reaction is named after the chemists Francis Robert Japp and Felix Klingemann, who first reported it in 1887. | ||
==Reaction | ==Reaction mechanism== | ||
The Japp–Klingemann reaction involves the | The Japp–Klingemann reaction involves the coupling of an aryl diazonium salt with a _-keto acid or its ester to form a hydrazone. The general mechanism can be described in the following steps: | ||
# '''Formation of the diazonium salt''': An [[aromatic amine]] is treated with [[nitrous acid]] to form the corresponding aryl diazonium salt. | |||
# '''Coupling reaction''': The aryl diazonium salt reacts with a _-keto acid or its ester. This step involves the nucleophilic attack of the _-keto compound on the diazonium ion, leading to the formation of a hydrazone intermediate. | |||
# '''Hydrazone formation''': The intermediate undergoes tautomerization to form the stable hydrazone product. | |||
[[File:Japp-Klingemann_reaction.png|thumb|right|300px|General scheme of the Japp–Klingemann reaction.]] | |||
==Applications== | ==Applications== | ||
The | The Japp–Klingemann reaction is particularly useful in the synthesis of [[azo compound]]s and [[hydrazone]]s, which are important intermediates in the production of dyes, pigments, and pharmaceuticals. The reaction is valued for its ability to introduce a hydrazone functional group into a molecule, which can be further manipulated in subsequent synthetic steps. | ||
==Advantages and limitations== | |||
The Japp–Klingemann reaction is advantageous due to its simplicity and the availability of starting materials. However, it has some limitations, including: | |||
* '''Selectivity''': The reaction may lead to mixtures of products if multiple reactive sites are present. | |||
The | * '''Stability of diazonium salts''': Aryl diazonium salts can be unstable and may decompose, especially at higher temperatures. | ||
== | ==Related reactions== | ||
The Japp–Klingemann reaction is related to other diazonium coupling reactions, such as the [[Sandmeyer reaction]] and the [[Gattermann reaction]], which also involve the use of diazonium salts in organic synthesis. | |||
==See | ==See also== | ||
* [[Diazonium compound]] | |||
* [[Azo coupling]] | |||
* [[Hydrazone]] | * [[Hydrazone]] | ||
* [[ | * [[Organic synthesis]] | ||
== | ==Related pages== | ||
* [[Sandmeyer reaction]] | |||
* [[Gattermann reaction]] | |||
* [[Azo compound]] | |||
[[Category:Organic reactions]] | [[Category:Organic reactions]] | ||
[[Category:Name reactions]] | [[Category:Name reactions]] | ||
Revision as of 17:33, 18 February 2025
A chemical reaction used in organic synthesis
The Japp–Klingemann reaction is a chemical reaction used in organic chemistry to synthesize hydrazones from aryl diazonium salts and _-keto acids or their esters. This reaction is named after the chemists Francis Robert Japp and Felix Klingemann, who first reported it in 1887.
Reaction mechanism
The Japp–Klingemann reaction involves the coupling of an aryl diazonium salt with a _-keto acid or its ester to form a hydrazone. The general mechanism can be described in the following steps:
- Formation of the diazonium salt: An aromatic amine is treated with nitrous acid to form the corresponding aryl diazonium salt.
- Coupling reaction: The aryl diazonium salt reacts with a _-keto acid or its ester. This step involves the nucleophilic attack of the _-keto compound on the diazonium ion, leading to the formation of a hydrazone intermediate.
- Hydrazone formation: The intermediate undergoes tautomerization to form the stable hydrazone product.
Applications
The Japp–Klingemann reaction is particularly useful in the synthesis of azo compounds and hydrazones, which are important intermediates in the production of dyes, pigments, and pharmaceuticals. The reaction is valued for its ability to introduce a hydrazone functional group into a molecule, which can be further manipulated in subsequent synthetic steps.
Advantages and limitations
The Japp–Klingemann reaction is advantageous due to its simplicity and the availability of starting materials. However, it has some limitations, including:
- Selectivity: The reaction may lead to mixtures of products if multiple reactive sites are present.
- Stability of diazonium salts: Aryl diazonium salts can be unstable and may decompose, especially at higher temperatures.
Related reactions
The Japp–Klingemann reaction is related to other diazonium coupling reactions, such as the Sandmeyer reaction and the Gattermann reaction, which also involve the use of diazonium salts in organic synthesis.
