Kolbe–Schmitt reaction
| Kolbe–Schmitt reaction | |
|---|---|
| Named after | |
| Reaction type | Addition reaction |
| Identifiers | |
| Organic Chemistry Portal | kolbe-schmitt-reaction |
| RSC ontology ID | RXNO:0000182 |
The Kolbe–Schmitt reaction or Kolbe process (named after Hermann Kolbe and Rudolf Schmitt) is a carboxylation chemical reaction that proceeds by treating phenol with sodium hydroxide to form sodium phenoxide,[1] then heating sodium phenoxide 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).[2][3][4][5]
By using potassium hydroxide, 4-hydroxybenzoic acid is accessible, an important precursor for the versatile paraben class of biocides used e.g. in personal care products.
The methodology is also used in the industrial synthesis of 3-hydroxy-2-naphthoic acid; the regiochemistry of the carboxylation in this case is sensitive to temperature.[6]
Reaction mechanism
[edit]The Kolbe–Schmitt reaction proceeds via the nucleophilic addition of a phenoxide, classically sodium phenoxide (NaOC6H5), to carbon dioxide to give the salicylate. The final step is the reaction (protonation) of the salicylate anion with an acid to form the desired salicylic acids (ortho- and para- isomers).
References
[edit]- ^ C. S. Marvel; A. L. Tanenbaum (1929). "γ-Phenoxypropyl Bromide". Org. Synth. 9: 72. doi:10.15227/orgsyn.009.0072.
- ^ Hermann Kolbe (1860). "Ueber Synthese der Salicylsäure" [On the synthesis of salicylic acid]. Annalen der Chemie und Pharmacie. 113 (1): 125–127. doi:10.1002/jlac.18601130120. English translation by Matthew Johnathan Leonard.
- ^ R. Schmitt (1885). "Beitrag zur Kenntniss der Kolbe'schen Salicylsäure Synthese" [Contribution to [our] knowledge of Kolbe's synthesis of salicylic acid]. Journal für Praktische Chemie. 2nd series. 31 (1): 397–411. doi:10.1002/prac.18850310130.
- ^ A. S. Lindsey and H. Jeskey (1957). "The Kolbe-Schmitt Reaction". Chem. Rev. 57 (4): 583–620. doi:10.1021/cr50016a001. (Review)
- ^ R. T. Morrison and R. N. Boyd (1983). Organic Chemistry (4th ed.). Allyn and Bacon. p. 976-7. ISBN 0-205-05838-8.
- ^ Gerald Booth (2005). "Naphthalene Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_009. ISBN 3-527-30673-0..