Reactions of organocopper reagents

Reactions of organocopper reagents involve species containing copper-carbon bonds acting as nucleophiles in the presence of organic electrophiles. Organocopper reagents are now commonly used in organic synthesis as mild, selective nucleophiles for substitution and conjugate addition reactions.[1]

Since the discovery that copper(I) halides catalyze the conjugate addition of Grignard reagents in 1941,[2] organocopper reagents have emerged as weakly basic, nucleophilic reagents for substitution and addition reactions. The constitution of organocopper compounds depends on their method of preparation and the various kinds of organocopper reagents exhibit different reactivity profiles. As a result, the scope of reactions involving organocopper reagents is extremely broad.

Mechanism and Stereochemistry

Substitution Reactions

The mechanism of nucleophilic substitution by lower-order organocuprates depends in a profound way on the structure of the substrate, organocuprate, and reaction conditions. Early evidence suggested that a direct SN2 displacement was occurring;[6] however more recent results suggest that invertive oxidative addition of copper(I) into the carbon-leaving group bond takes place, generating a copper(III) intermediate which then undergoes reductive elimination to generate the coupled product.[7] Both of these mechanisms predict inversion at the electrophilic carbon, which is observed in a number of cases.[8] On the other hand, experiments with radical traps and the observation of racemization during substitution suggest a radical mechanism.[9]

(1)

Conjugate Addition Reactions

The mechanistic picture of conjugate additions of organocuprates is also complex. A significant amount of evidence has been gathered for the existence of an initial complex between the enone and the organocuprate.[10] Carbocupration across the carbon-carbon double bond may then generate a copper enolate, as shown at the bottom of Eq. (2). More likely, however, is conjugate addition of the organocuprate to afford a lithium enolate.[11] Subsequent reductive elimination and protonation leads to the product.[12]

(2)

Enantioselective Variants

Diastereoselective conjugate addition reactions of chiral organocuprates provide β-functionalized ketones in high yield and diastereoselectivity. A disadvantage of these reactions is the requirement of a full equivalent of enantiopure starting material.[13]

(3)

More recently, catalytic enantioselective methods have been developed based on the copper(I)-catalyzed conjugate addition of Grignard reactions to enones. The proposed mechanism involves transmetalation from the Grignard reagent to copper, conjugate addition, and rate-determining reductive elimination (see the analogous upper pathway in equation (2)).[14]

(4)

Scope and Limitations

Reactions of organocopper species can be divided into catalytic and stoichiometric variants. Although organocopper compounds have primarily been employed in stoichiometric amounts for organic synthesis, catalytic methods are useful for enantioselective reactions and require less preparation than stoichiometric methods. This section describes both catalytic and stoichiometric reactions of organocopper complexes, with a particular focus on nucleophilic substitution and conjugate addition reactions.

Catalytic Reactions of Organocopper Compounds

Vinyl and aryl Grignard reagents couple with primary alkyl halides in the presence of a catalytic amount of a copper(I) halide salt. The use of Li2CuCl4 rather than simple copper(I) halide salts (CuX) improves yields of these coupling reactions substantially.[15]

(5)

The addition of Grignard reagents to alkynes is facilitated by a catalytic amount of copper halide. Transmetalation to copper and carbocupration are followed by transmetalation of the product alkene back to magnesium. The addition is syn unless a coordinating group is nearby in the substrate, in which case the addition becomes anti and yields improve.[16]

(6)

Stoichiometric Reactions of Organocopper Compounds

Propargyl methanesulfinates are useful substrates for the synthesis of allenes from stoichiometric organocopper complexes. In this case, the complexes were generated in situ through the combination of a Grignard reagent, copper(I) bromide, and lithium bromide. Organocopper complexes very often need Lewis acid activation in order to react efficiently; magnesium bromide generated in situ serves as an activating Lewis acid in this case.[17]

(7)

Alkenylcopper complexes, easily generated through carbocupration, are useful for the introduction of a vinyl group in the β position of a carbonyl compound. In this case, as above, magnesium bromide is serving as an activating Lewis acid.[18]

(8)

Epoxide opening with organocuprates is highly selective for the less hindered position. Substitution takes place with complete inversion of configuration at the electrophilic carbon.[19]

(9)

Generally, organocuprates react with allylic electrophiles in an anti SN2 fashion. In the reaction below, nearly complete inversion of configuration was observed despite the presence of a second stereocenter in the ring.[20]

(10)

Conjugate addition of organocuprates is widely used in organic synthesis. Vinyl ether cuprates serve as convenient acyl anion equivalents in conjugate addition reactions to enones. The resulting enol ethers can be hydrolyzed to 1,4-diketones, which are difficult to access using conventional carbonyl chemistry.[21]

(11)

The use of additives in conjunction with a stoichiometric amount of organocopper complexes enhances the rate and yield of many reactions. Organocopper complexes in particular react sluggishly in the absence of a Lewis acid. Although magnesium bromide generated in situ from the reaction of Grignard reagents and copper(I) halides can serve this role (see above), external Lewis acids are also useful. In the presence of boron trifluoride etherate, organocopper complexes are able to add to sterically congested enones in moderate yield (effecting the same transformation with an organocuprate would be difficult).[22]

(12)

Boron trifluoride etherate is also useful as an additive in reactions of higher-order cyanocuprates. The use of the 2-thienyl group as a "dummy" substituent in the cyanocuprate conserves the potentially valuable organolithium reagent used to generate the cyanocuprate (as only the dummy group is present in copper-containing byproducts). In the absence of boron trifluoride etherate, no reaction was observed in this case.[23]

(13)

Conjugate addition reactions of higher-order cyanocuprates represent another useful application for boron trifluoride etherate. The vinyl group is transferred selectively in this reaction; this is in contrast to substitution reactions employing the same reagent, which result in selective transfer of the methyl group.[24]

(14)

Synthetic Applications

Because the stereoselectivity of carbocupration is extremely high, the reaction has been applied to the synthesis of pheromones in which the geometric purity of double bonds is critical. One example is the insect pheromone of Cossus cossus, which is synthesized by syn-selective carbocupration of acetylene and alkylation of the resulting organocuprate in the presence of added phosphite.[25]

(15)

References

  1. 1 2 Lipshutz, B. H.; Sengupta, S. Org. React. 1992, 41, 135. doi:10.1002/0471264180.or041.02
  2. ↑ Kharasch, M. S.; Tawney, P. O. J. Am. Chem. Soc. 1941, 63, 2308.
  3. ↑ Kansal, V. K.; Taylor, R. J. K. J. Chem. Soc. Perkin Trans. 1 1984, 703.
  4. ↑ Posner, G. H. Org. React. 1975, 22, 253.
  5. ↑ Lipshutz, B. H.; Wilhelm, R. S.; Floyd, D. M. J. Am. Chem. Soc. 1981, 103, 7672.
  6. ↑ Tamura, M.; Kochi, J. K. J. Organomet. Chem. 1972, 42, 205.
  7. ↑ Corey, E. J.; Boaz, N. W. Tetrahedron Lett. 1984, 25, 3059.
  8. ↑ Johnson, C. R.; Dutra, G. A. J. Am. Chem. Soc. 1973, 95, 7777.
  9. ↑ Ashby, E. C.; Coleman, D. J. Org. Chem. 1987, 52, 4554.
  10. ↑ Four, P.; Riviere, H.; Tang, P. W. Tetrahedron Lett. 1977, 3879.
  11. ↑ Krauss, S. R.; Smith, S. G. J. Am. Chem. Soc. 1981, 103, 141.
  12. ↑ Woodward, S. Chem. Soc. Rev. 2000, 29, 393.
  13. ↑ Malmberg, H.; Nilsson, M.; Ullenius, C. Tetrahedron Lett. 1982, 23, 3823.
  14. ↑ Harutyunyan, S.; López, F.; Browne, W.; Correa, A.; Peña, D.; Badorrey, R.; Meetsma, A.; Minnaard, A.; Feringa, B. L. J. Am. Chem. Soc. 2006, 128, 9103.
  15. ↑ Nunomoto, S.; Kawakami, Y.; Yamashita, Y. J. Org. Chem. 1983, 48, 1912.
  16. ↑ Jousseaume, B. Ph.D. Thesis, University of Bordeaux, France, 1977.
  17. ↑ Kleijn, H.; Elsevier, C. J.; Westmijze, H.; Meijer, J.; Vermeer, P. Tetrahedron Lett. 1979, 3101.
  18. ↑ Marfat, A.; McGuirk, P. R.; Helquist, P. J. Org. Chem. 1979, 44, 3888.
  19. ↑ Johnson, M. R.; Nakata, T.; Kishi, Y. Tetrahedron Lett. 1979, 4343.
  20. ↑ Goering, H. L.; Kantner, S. S. J. Org. Chem. 1981, 46, 2144.
  21. ↑ Boeckman, R. K.; Ramaiah, M. J. Org. Chem. 1977, 42, 1581.
  22. ↑ Yamamoto, Y.; Yamamoto, S.; Yatagai, S.; Ishihara, Y.; Maruyama, K. J. Org. Chem. 1982, 47, 119.
  23. ↑ Lipshutz, B. H.; Parker, D. A.; Kozlowski, J. A.; Nguyen, S. L. Tetrahedron Lett. 1984, 25, 5959.
  24. ↑ Lipshutz, B. H.; Wilhelm, R. S.; Kozlowski, J. A. J. Org. Chem. 1984, 49, 3938.
  25. ↑ Cahiez, G.; Alexakis, A.; Normant, J. F. Tetrahedron Lett. 1978, 2027.
This article is issued from Wikipedia - version of the Sunday, December 07, 2014. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.