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McMurry reaction

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Subject: Nicolaou Taxol total synthesis, McMurry, Ketyl, Pinacol coupling reaction, Barton–Kellogg reaction
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McMurry reaction

The McMurry reaction of benzophenone
The McMurry reaction is an ketone or aldehyde groups are coupled to an alkene using titanium chloride compound such as titanium(III) chloride and a reducing agent.[1] The reaction is named after its co-discoverer, John E. McMurry. The McMurry reaction originally involved the use of a mixture TiCl3 and LiAlH4, which produces the active reagent(s). Related species have been developed involving the combination of TiCl3 or TiCl4 with various other reducing agents, including potassium, zinc, and magnesium.[2][3] This reaction is related to the Pinacol coupling reaction which also proceeds by reductive coupling of carbonyl compounds.

Contents

  • Reaction mechanism 1
  • Background and scope 2
  • References 3
  • External links 4

Reaction mechanism

This reductive coupling can be viewed as involving two steps. First is the formation of a pinacolate (1,2-diolate) complex, a step which is equivalent to the pinacol coupling reaction. The second step is the deoxygenation of the pinacolate which yields the alkene. The second step exploits the oxophilicity of titanium.

A proposed mechanism when TiCl4 and Zn(Cu) are used for the coupling of benzophenone, as proposed in a reference.[4] Note that the mechanism may vary when different conditions are used.

Several mechanisms have been discussed for this reaction.[4] Low-valent titanium species induce coupling of the carbonyls by single electron transfer to the carbonyl groups. The required low-valent titanium species are generated via reduction, usually with zinc powder. This reaction is often performed in THF because it solubilizes intermediate complexes, facilitates the electron transfer steps, and is not reduced under the reaction conditions. The nature of low-valent titanium species formed is varied as the products formed by reduction of the precursor titanium halide complex will naturally depend upon both the solvent (most commonly THF or DME) and the reducing agent employed: typically, lithium aluminum hydride,zinc-copper couple, zinc dust, magnesium-mercury amalgam, magnesium, or alkali metals.[5] Bogdanovic and Bolte identified the nature and mode of action of the active species in some classical McMurry systems,[6] and an overview of proposed reaction mechanisms has been published.[4] It is of note that titanium dioxide is not generally a product of the coupling reaction. Although it is true that titanium dioxide is usually the eventual fate of titanium used in these reactions, it is generally formed upon the aqueous workup of the reaction mixture.[5]

Background and scope

The original publication by Mukaiyama demonstrated reductive coupling of ketones using reduced titanium reagents.[7] McMurry and Fleming coupled retinal to give carotene using a mixture of titanium trichloride and lithium aluminium hydride. Other symmetrical alkenes were prepared similarly, e.g. civetone from adamantanone and tetraphenylethylene from benzophenone. A McMurry reaction using titanium tetrachloride and zinc is employed in the synthesis of a first-generation molecular motor.[8]

McMurry coupling to a molecular motor

In another example, the Nicolaou's total synthesis of Taxol uses this reaction, although coupling stops with the formation of a cis-diol, rather than an olefin. Optimized procedures employ the dimethoxyethane complex of TiCl3 in combination with the Zn(Cu).

References

  1. ^
  2. ^ Ian C. Richards "Titanium(IV) Chloride–Zinc" in Encyclopedia of Reagents for Organic Synthesis, John Wiley, London, 2001. doi:10.1002/047084289X.rt125. Article Online Posting Date: April 15, 2001
  3. ^ Martin G. Banwell, "Titanium(III) Chloride–Lithium Aluminum Hydride" in Encyclopedia of Reagents for Organic Synthesis John Wiley, London, 2001. doi:10.1002/047084289X.rt129. Article Online Posting Date: April 15, 2001
  4. ^ a b c
  5. ^ a b
  6. ^
  7. ^ Mukaiyama, T.; Sato, T.; Hanna, "Reductive Coupling of Carbonyl Compounds to Pinacols and Olefins by Using TiCl4 and Zn" Chem. Lett. 1973, 1041. doi:10.1246/cl.1973.1041
  8. ^

External links

  • McMurry reaction in organic-chemistry.org
  • Mcmurry reaction at the University of Sussex
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