Wacker process



The Wacker process or the Hoechst-Wacker process (named after the chemical companies of the same name) originally referred to the oxidation of ethylene to heterogeneous catalyst.

Reaction mechanism

The modern understanding of the reaction mechanism for the Wacker process (olefin oxidation via palladium(II) chloride) is described below:

The catalytic cycle can be described as follows:

\mathrm{[PdCl_4]^{2-} + C_2H_4 + H_2O \rightarrow CH_3CHO + Pd + 2HCl +2Cl^-}
\mathrm{Pd + 2CuCl_2 + 2Cl^- \rightarrow [PdCl_4]^{2-} + 2CuCl}
\mathrm{2CuCl + 1/2O_2 + 2HCl \rightarrow 2CuCl_2 + H_2O}

Note that all catalysts are regenerated and only the alkene and oxygen are consumed. Without CuCl back to CuCl2, allowing the cycle to repeat.

The initial stoichiometric reaction was first reported by Phillips[2][3] and the The Wacker reaction was first reported by Smidt et al.[4].[5][6]

Mechanism summary

Substantial mechanistic investigation on the olefin oxidation cycle has elucidated much of the oxidation process, though some questions remain.[7] Several interesting key points were found:

(1) there is no H/D exchange seen in this reaction. Reaction runs with C2D4 in water generate CD3CDO, and runs with C2H4 in D2O generate CH3CHO. Thus, keto-enol tautomerization is not a possible mechanistic step.

(2) There is a negligible kinetic isotope effect with fully deuterated reactants (k H/k D=1.07). Hence, it is inferred that hydride transfer is not a rate-determining step.

(3) a significant competitive isotope effect with C2H2D2, (k H/k D= ~1.9), suggests that the rate determining step should be prior to oxidized product formation.

For these reasons, modern understanding of this process has the rate-determining step occurring before a series of hydride rearrangements. However, it has been recognized that experimental conditions play a crucial role in which mechanistic pathway is taken.

The bulk of mechanistic studies on the Wacker Process debated whether nucleophilic attack occurred via an external (anti-addition) pathway or via an internal (syn-addition) pathway. Studies by Stille and coworkers[8][9][10] apparently suggested that the Wacker Process proceeds via anti-addition, however these studies have been refuted as they assumed that changes in reaction conditions do not influence the reaction mechanism. However, other contemporary studies in high chloride concentration conditions also concluded that nucleophilic attack was an anti-addition reaction.[11] Numerous textbooks have erroneously propagated these studies as proof that the reaction occurs via an anti-addition step when in fact the mechanism is more complicated. Subsequent stereochemical studies by Patrick M. Henry and coworkers confirmed that both pathways occur and are dependent on chloride concentrations.[12][13]

In summary, it was determined that syn-addition occurs under low-chloride reaction concentrations (< 1 mol/L, industrial process conditions), while anti-addition occurs under high-chloride (> 3 mol/L) reaction concentrations. However, the exact pathway and the reason for this switching of pathways is still unknown.

Another key step in the Wacker process is the migration of the hydrogen from oxygen to chlorine and formation of the C-O double bond. This step is generally regarded to proceed through a so-called β-hydride elimination with a four-membered cyclic transition state:

One in silico study[14] argues that the reaction mechanism in which the proton directly attaches itself to chlorine with an activation energy of 18.8 kcal/mol. The proposed reaction step gets assistance from a water molecule acting as a catalyst.

Wacker-Tsuji oxidation

The so-called Wacker-Tsuji oxidation is the laboratory scale version of the above reaction, for example the conversion of dimethylformamide solvent mixture in the presence of air[15]

References

  1. ^ Translated in part from de:Wacker-Verfahren.
  2. ^ F.C. Phillips, Am. Chem. J., 1894, 16, 255-277.
  3. ^ F.C. Phillips, Z. Anorg. Chem., 1894, 6, 213-228.
  4. ^ J. Smidt, W. Hafner, R. Jira, J. Sedlmeier, R. Sieber, R. Rüttinger, and H. Kojer, Angew. Chem., 1959, 71, 176-182.
  5. ^ W. Hafner, R. Jira, J. Sedlmeier, and J. Smidt, Chem. Ber., 1962, 95, 1575-1581.
  6. ^ J. Smidt, W. Hafner, R. Jira, R. Sieber, J. Sedlmeier, and A. Sabel, Angew. Chem., Int. Ed. Engl., 1962, 1, 80-88.
  7. ^ Henry, Patrick M. In Handbook of Organopalladium Chemistry for Organic Synthesis; Negishi, E., Ed.; Wiley & Sons: New York, 2002; p 2119. ISBN 0471315060
  8. ^ James, D.E., Stille, J.K. J. Organomet. Chem., 1976, 108, 401. doi:10.1021/ja00423a028
  9. ^ Stille, J.K., Divakarumi, R.J., J. Organomet. Chem., 1979, 169, 239;
  10. ^ James, D.E., Hines, L.F., Stille, J.K. J. Am. Chem. Soc., 1976, 98, 1806 doi:10.1021/ja00423a027
  11. ^ Baeckvall, J.E., Akermark, B., Ljunggren, S.O., J. Am. Chem. Soc., 1979, 101, 2411. doi:10.1021/ja00503a029
  12. ^ Francis, J.W., Henry, P.M. Organometallics, 1991, 10, 3498. doi:10.1021/om00056a019
  13. ^ Francis, J.W., Henry, P.M. Organometallics, 1992, 11, 2832.doi:10.1021/om00044a024
  14. ^ Inaccessibility of -Hydride Elimination from -OH Functional Groups in Wacker-Type Oxidation John A. Keith, Jonas Oxgaard, and William A. Goddard, III J. Am. Chem. Soc.; 2006; 128(10) pp 3132 - 3133; doi:10.1021/ja0533139
  15. ^ Jiro Tsuji, Hideo Nagashima, and Hisao Nemoto, General Synthetic Method for the preparation of Methyl Ketones from Terminal Olefins: 2-Decanone, Organic Syntheses, Coll. Vol. 7, p.137 (1990); Vol. 62, p.9 (1984).
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Wacker_process". A list of authors is available in Wikipedia.