Bis(cyclopentadienyl)zirconium chloride hydride

Bis(cyclopentadienyl)zirconium chloride hydride Basic information
Reaction
Product Name:Bis(cyclopentadienyl)zirconium chloride hydride
Synonyms:ZIRCONOCENE CHLORIDE HYDRIDE;Di(cyclopentadienyl)zirconium(IV) chloride hydride;bis(3-cyclopentadienyl)chlorohydrurozirconium;Bis(cyclopentadienyl)zirconium chloride hydride (Schwartz's Reagent),;Bis(cyclopentadienyl)zirconiumchloridehydride~Schwartz'sReagent~Zirconocenehydrochloride;Zirconocenechloridehydride,95%;Bis(cyclopentadienyl)zirconiumchloridehydride(Schwartz'sReagent),95%;Di(cyclopentadienyl)zirconium(IV) chloride hydride, Schwartz reagent, Zirconocene chloride hydride
CAS:37342-97-5
MF:C10H11ClZr
MW:257.87
EINECS:253-479-5
Product Categories:Zr;Classes of Metal Compounds;Metallocenes;Reduction;Synthetic Organic Chemistry;Titanocene, etc.;Transition Metal Compounds;Zr (Zirconium) Compounds;Auxiliaries,Catalysts
Mol File:37342-97-5.mol
Bis(cyclopentadienyl)zirconium chloride hydride Structure
Bis(cyclopentadienyl)zirconium chloride hydride Chemical Properties
Melting point 300 °C
storage temp. Keep in dark place,Inert atmosphere,2-8°C
form Powder
color off-white
Water Solubility reacts
Sensitive Light, Air & Moisture Sensitive
Hydrolytic Sensitivity8: reacts rapidly with moisture, water, protic solvents
Merck 14,8396
Exposure limitsACGIH: TWA 5 mg/m3; STEL 10 mg/m3
NIOSH: IDLH 25 mg/m3; TWA 5 mg/m3; STEL 10 mg/m3
CAS DataBase Reference37342-97-5(CAS DataBase Reference)
Safety Information
Hazard Codes F,C
Risk Statements 11-15-34
Safety Statements 16-26-27-36/37/39-8-45
RIDADR UN 3131 4.3/PG 2
WGK Germany 3
8-10-23
HazardClass 4.3
PackingGroup II
HS Code 29319090
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Bis(cyclopentadienyl)zirconium chloride hydride Usage And Synthesis
Reaction
  1. Reagent for the hydrozirconation of olefins.
  2. Reagent for the hydrozirconation of alkynes.
  3. Catalyst for the hydroboration of olefins.
  4. Mediates the reduction of tertiary amides to aldehydes, without reduction of cyano, nitro, ester, or α,β-unsaturated groups.
  5. Catalyst for the asymmetric vinylation and dienylation of ketones.
  6. Useful reagent for dimethylzinc mediated additions alkenylzirconocenes to aldimines.
  7. Useful reagent for the synthesis of oxidized amides from nitriles.
  8. Reagent for the hydrozirconation of propargylic alcohols.
Reactions of 37342-97-5_1
Reactions of 37342-97-5_2
Reactions of 37342-97-5_3

Chemical Propertieswhite to beige powder
UsesFunctionalization of unsaturated systems via an organozirconium intermediate.
UsesBis(cyclopentadienyl)zirconium hydridochloride is used in the conversion of amides to aldehydes. It is also used as a pharmaceutical intermediate.
Purification MethodsIt is moisture and light sensitive. Determine its purity by reaction with a slight excess of Me2CO whereby the active H reacts to produce Cp2ZrClOPri and the integrals of the residual Me2CO in the 1H NMR will show its purity. The presence of Cp2ZrH2 can be determined because it forms Cp2Zr(OPri)2. For a very active compound, it is best to prepare it freshly from the dichloride (see below) by reduction with Vitride [LiAl(OCH2CH2OH)2H2], the white precipitate is filtered off, washed with tetrahydrofuran, then Et2O and dried in a vacuum. Store it dry in the dark. [Carr & Schwartz J Am Chem Soc 101 3521 1979, Negishi & Takahashi Synthesis 1 1988, Beilstein 16 IV 1770.]
Bis(cyclopentadienyl)zirconium chloride hydride Preparation Products And Raw materials
Raw materialsTetrahydrofuran-->Sodium-->Toluene-->Lithium Aluminum Hydride-->Carbon tetrachloride-->1,3-Cyclopentadiene-->Zirconium tetrachloride
Zirconium dioxide Benzyl chloride polydicyclopentadiene Zirconium hydroxide Calcium chloride Bis(cyclopentadienyl)zirconium dichloride Dicyclopentadiene Hydrochlorothiazide Tetrahydrocyclopentadiene Choline chloride Ammonium chloride Mepiquat chloride Zirconium sulphate Polyvinyl chloride METHYLCYCLOPENTADIENE DIMER 2-​[[(2-​ethylphenyl)​(2-​hydroxyethyl)​amino]​methyl]​-​3,​3-​difluoro-Propanenitrile Zirconyl chloride octahydrate 1,3-Cyclopentadiene Schwartz Reagent

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