Seyferth-Gilbert homologation
From Wikipedia, the free encyclopedia
The Seyferth-Gilbert homologation is a the chemical reaction of an aryl ketone 1 (or aldehyde) with dimethyl (diazomethyl)phosphonate 2 and potassium tert-butoxide to give substituted alkynes 3. Dimethyl (diazomethyl)phosphonate 2 is often called the Seyferth-Gilbert reagent.
This reaction is called a homologation because the product has exactly one additional carbon more than the starting material.
Contents |
[edit] Reaction mechanism
Deprotonation of the Seyferth-Gilbert reagent A give an anion B which reacts with the ketone to form the oxaphosphatane D. Elimination of dimethylphosphate E gives the vinyl diazo-intermediate Fa and Fb. The generation of nitrogen gas gives a vinyl carbene G which via a 1,2-migration forms the desired alkyne H.
[edit] Bestmann modification
Dimethyl (diazomethyl)phosphonate can be generated in situ from dimethyl-1-diazo-2-oxopropylphosphonate (also called Bestmann's reagent) by reaction with methanol and potassium carbonate. Reaction of Bestmann's reagent with aldehydes gives terminal alkynes often in very high yield.
The use of the milder potassium carbonate makes this procedure much more compatible with a wide variety of functional groups.
[edit] References
- ↑ Seyferth, D.; Marmor, R. S.; Hilbert, P. J. Org. Chem. 1971, 36, 1379-1386. (DOI:10.1021/jo00809a014)
- ↑ Gilbert, J. C.; Weerasooriya, U. J. Org. Chem. 1982, 47, 1837-1845. (DOI:10.1021/jo00349a007)
- ↑ Brown, D. G.; Velthuisen, E. J.; Commerford, J. R.; Brisbois, R. G.; Hoye, T. H. J. Org. Chem. 1996, 61(7), 2540-2541. (DOI:10.1021/jo951944n)
- ↑ Müller, S.; Liepold, B.; Roth, G. J.; Bestmann, H. J. Synlett 1996, 521.
- ↑ Roth, G. J.; Liepold, B.; Müller, S. G.; Bestmann, H. J. Synthesis 2004, 59-62. (Abstract)
