The Kolbe-Schmitt reaction/Kolbe process (named after Adolph Wilhelm Hermann Kolbe and Rudolf 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).[1][2][3]
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.
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.
References
- ^ Hermann Kolbe (1860). "Ueber Synthese der Salicylsäure". Annalen der Chemie und Pharmacie 113 (1): 125–127. doi:.
- ^ R. Schmitt (1885). "Beitrag zur Kenntniss der Kolbe'schen Salicylsäure Synthese". Journal für Praktische Chemie 31 (1): 397–411. doi:.
- ^ A. S. Lindsey and H. Jeskey (1957). "The Kolbe-Schmitt Reaction". Chem. Rev. 57 (4): 583–620. doi:. (Review)
This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see full disclaimer)
