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Schwartz's reagent

Schwartz's reagent
IUPAC name Bis(η5-cyclopentadienyl)- zirconium(IV) chloride hydride
Other names Cp2ZrClH, zirconocene chloride hydride
CAS number 37342-97-5
Molecular formula C10H11Cl Zr
Molar mass 257.87 g/mol
Appearance White solid
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Schwartz's reagent is the common name for the chemical compound with the formula (C5H5)2ZrHCl. This metallocene is used in organic synthesis for various transformations of alkenes and alkynes.[1][2][3]

Additional recommended knowledge


Schwartz's reagent reacts with alkenes and alkynes via the process called hydrozirconation which formally results in the addition of the Zr-H bond across the C=C or C≡C bond. The selectivity of the hydrozirconation of alkynes has been studied in detail.[4][5] The rate of addition to unsaturated carbon-carbon bonds is terminal alkyne > terminal alkene ~ internal alkyne > disubstituted alkene.[6] Acyl complexes can be generated by insertion of CO into the C-Zr bond resulting from hydrozirconation.[7]


The complex was first prepared by Wailes and Weigold.[8] It can be purchased or readily prepared by reduction of zirconocene dichloride with lithium aluminum hydride.[9]

(C5H5)2ZrCl2 + 1/4 LiAlH4 → (C5H5)2ZrHCl + 1/4 "LiAlCl4"

In practice this reaction also makes (C5H5)2ZrH2, which is treated with methylene chloride to give the mixed hydride chloride. An alternative procedure that generated Schwartz'd Reagent from dihydride has also been reported.[10]

It is claimed that Schwartz's Reagent has been used in over 100 natural product syntheses.[11]


  1. ^ D. W. Hart and J. Schwartz (1974). "Hydrozirconation. Organic Synthesis via Organozirconium Intermediates. Synthesis and Rearrangement of Alkylzirconium(IV) Complexes and Their Reaction with Electrophiles". J. Am. Chem. Soc. 96 (26): 8815-8116. doi:10.1021/ja00833a048.
  2. ^ J. Schwartz, and J. A. Labinger (2003). "Hydrozirconation: A New Transition Metal Reagent for Organic Synthesis". Angew. Chem. Int. Ed. 15 (6): 330-340. doi:10.1002/anie.197603331.
  3. ^ Donald W. Hart, Thomas F. Blackburn, Jeffrey Schwartz (1975). "Hydrozirconation. III. Stereospecific and regioselective functionalization of alkylacetylenes via vinylzirconium(IV) intermediates". J. Am. Chem. Soc. 97 (3): 679-680. doi:10.1021/ja00836a056.
  4. ^ R. C. Sun, M. Okabe, D. L. Coffen, and J. Schwartz (1998). "Conjugate Addition of a Vinylzirconium Reagent: 3-(1-Octene-1-yl)cyclopentanone". Org. Synth.; Coll. Vol. 9: 640. 
  5. ^ Panek, J. S.; Hu, T. (1997). "Stereo- and Regiocontrolled Synthesis of Branched Trisubstituted Conjugated Dienes by Palladium(0)-Catalyzed Cross-Coupling Reaction". J. Org. Chem. 62 (15): 4912-4913. doi:10.1021/jo970647a.
  6. ^ Peter Wipf and Heike Jahn (1996). "Synthetic applications of organochlorozirconocene complexes". Tetrahedron 52 (40): 12853-12910. doi:10.1016/0040-4020(96)00754-5.
  7. ^ Christopher A. Bertelo, Jeffrey Schwartz (1975). "Hydrozirconation. II. Oxidative homologation of olefins via carbon monoxide insertion into the carbon-zirconium bond". J. Am. Chem. Soc. 97 (1): 228-230. doi:10.1021/ja00834a061.
  8. ^ P. C. Wailes and H. Weigold (1970). "Hydrido complexes of zirconium I. Preparation". Journal of Organometallic Chemistry 24: 405-411. doi:10.1016/S0022-328X(00)80281-8.
  9. ^ S. L. Buchwald, S. J. LaMaire, R. B. Nielsen, B. T. Watson, and S. M. King. "Schwartz's Reagent". Org. Synth.; Coll. Vol. 9: 162. 
  10. ^ Peter Wipf, Hidenori Takahashi, and Nian Zhuang (1998). "Kinetic vs. thermodynamic control in hydrozirconation reactions". Pure Appl. Chem. 70 (5): 1077-1082.
  11. ^ A. Maureen Rouhi (1998). "Organozirconium Chemistry Arrives". C&EN News 82 (16): 162.
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Schwartz's_reagent". A list of authors is available in Wikipedia.
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