Pechmann condensation

The Pechmann condensation is a synthesis of coumarins, starting from a phenol and a carboxylic acid or ester containing a β-carbonyl group.[1] The condensation is performed under acidic conditions. The mechanism involves an esterification/transesterification followed by attack of the activated carbonyl ortho to the oxygen to generate the new ring. The final step is a dehydration, as seen following an aldol condensation. It was discovered by the German chemist Hans von Pechmann [2] .

Pechmann condensation
Named after Hans von Pechmann
Reaction type Ring forming reaction
Identifiers
Organic Chemistry Portal pechmann-condensation

With simple phenols, the conditions are harsh, although yields may still be good.[3]

The Pechmann condensation as applied to 4-methylcoumarin

With highly activated phenols such as resorcinol, the reaction can be performed under much milder conditions. This provides a useful route to umbelliferone derivatives:

The Pechmann condensation as applied to 7-hydroxy-4-methylcoumarin

For coumarins unsubstituted at the 4-position, the method requires the use of formylacetic acid or ester. These are unstable and not commercially available, but the acid may be produced in situ from malic acid and sulfuric acid above 100 °C. As soon as it forms, the formylacetic acid performs the Pechmann condensation. In the example shown, umbelliferone itself is produced, albeit in low yield:

The Pechmann condensation as applied to umbelliferone

Mechanistic studies

The mechanism of the reaction has been studied in details with theoretical treatment.[4]

The study shown that reaction takes place on oxo-form, and not on enolic-form. Three different oxo-routes have been proposed.

Simonis chromone cyclization

In a variation the reaction of phenols and beta-ketoesters and phosphorus pentoxide yields a chromone. This reaction is called Simonis chromone cyclization.[5][6] The ketone in the ketoester is activated by P2O5 for reaction with the phenol hydroxyl group first, the ester group in it is then activated for electrophilic attack of the arene.

gollark: Why?
gollark: osmarkswebprograms™ always work well, reliably and fast.
gollark: I can do it for you.
gollark: V5 is Mini.
gollark: We don't even have a V6.

See also

References
  1. J. A. Joule, K. Mills Heterocyclic Chemistry, 4th edition, Blackwell Science, Oxford, UK, 2000.
  2. H. v. Pechmann (1884). "Neue Bildungsweise der Cumarine. Synthese des Daphnetins". Berichte der deutschen chemischen Gesellschaft. 17 (1): 929–936. doi:10.1002/cber.188401701248.
  3. Eugene H. Woodruff , Organic Syntheses, Coll. Vol. 3, p.581. Available online Archived 2011-05-14 at the Wayback Machine.
  4. Daru, János; Stirling, András (4 November 2011). "Mechanism of the Pechmann Reaction: A Theoretical Study". The Journal of Organic Chemistry. 76 (21): 8749–8755. doi:10.1021/jo201439u. PMID 21932799.
  5. E. Petschek, H. Simonis, Ber. 46, 2014 (1913).
  6. Name reactions: a collection of detailed reaction mechanisms, Jie Jack Li
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.