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Reformatsky reaction

 
Wikipedia: Reformatsky reaction

The Reformatsky reaction (sometimes spelled Reformatskii reaction) is an organic reaction which condenses aldehydes (or ketones), 1, with α-halo esters, 2, using a metallic zinc catalyst to form β-hydroxy-esters, 3.[1][2] It was discovered by Sergei Nikolaevich Reformatskii.

The Reformatskii reaction

The organozinc reagent, also called a 'Reformatskii enolate', is prepared by treating an alpha-halo ester with zinc dust. Reformatskii enolates are less reactive than lithium enolates or Grignard reagents and hence nucleophilic addition to the ester group does not occur.

Some reviews have been published.[3][4]

Contents

Structure of the reagent

The crystal structures of the THF complexes of the Reformatsky reagents tert-butyl bromozincacetate[1] and ethyl bromozincacetate[2] have been determined. Both form cyclic eight-membered dimers in the solid state, but differ in stereochemistry: the eight-membered ring in the ethyl derviative adopts a tub-shaped conformation and has cis bromo groups and cis THF ligands, whereas in the tert-butyl derviative, the ring is in a chair form and the bromo groups and THF ligands are trans.

Ethyl-bromozincacetate-from-xtal-3D-sticks-C.png
Ethyl-bromozincacetate-THF-dimer-from-xtal-2D-skeletal-D.png
Tert-butyl-bromozincacetate-from-xtal-3D-sticks-C.png
Tert-butyl-bromozincacetate-THF-dimer-from-xtal-2D-skeletal-D.png
ethyl bromozincacetate dimer
tert-butyl bromozincacetate dimer

Variations

In one variation of the Reformatsky reaction[5] an iodolactone is coupled with an aldehyde with triethylborane in toluene at -78°C.

Reformatsky reaction Danishefsky variation ref. Lambert 2006


See also

References

  1. ^ J. Dekker, P. H. M. Budzelaar, J. Boersma, G. J. M. Van der Kerk, A. J. Spek (1984). Organometallics 9 (3): 1403–1407. doi:10.1021/om00087a015. 
  2. ^ S. Miki, K. Nakamoto, J. Kawakami, S. Handa, S. Nuwa (2008). Synthesis: 409–412. doi:10.1055/s-2008-1032023. 

Bibliography

  1. ^  Reformatskii, S., Neue Synthese zweiatomiger einbasischer Säuren aus den Ketonen, Ber. 1887, 20, 1210. doi:10.1002/cber.188702001268
  2. ^  Reformatskii, S. J. Russ. Phys. Chem. Soc. 1890, 22, 44.
  3. ^  Shriner, R. L. Org. React. 1942, 1, 1. (Review)
  4. ^  Rathke, M. W. Org. React. 1975, 22, 423. (Review)
  5. ^  Total Synthesis of UCS1025A Tristan H. Lambert and Samuel J. Danishefsky J. Am. Chem. Soc. 2006, 128(2), 426 - 427. (Communication) doi:10.1021/ja0574567 Abstract

See also


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