Kolbe-Schmitt reaction
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The Kolbe-Schmitt reaction/Kolbe process (named after Adolph Wilhelm Hermann Kolbe and R. Schmitt) is a carboxylation chemical reaction that proceeds by heating sodium phenolate (the sodium salt of phenol) with carbon dioxide under pressure (100 atm, 125°C), then treating the product with sulfuric acid. The final product is an aromatic hydroxy acid which is also known as salicylic acid (the precursor to aspirin).
By using the potassium salt 4-hydroxybenzoic acid is accessible, an important precursor for the versatile paraben class of biocides used e.g. in personal care products.
[edit] Reaction mechanism
The Kolbe-Schmitt reaction proceeds via the nucleophilic addition of a phenolate to carbon dioxide to give the salicylate. The final step is reaction of the salicylate with acid to form the desired salicylic acid.
[edit] References
- Kolbe, H. Ann. 1860, 113, 125.
- Schmitt, R. J. Prakt. Chem. 1885, [2] 31, 397.
- Lindsey, A. S.; Jeskey, H. Chem. Rev. 1957, 57(4), 583-620. (Review)
