HCID 178418348, compound → HCID 92002078, compound

HRID 412837Notes

Reaction equation

HRID 412837 reaction equation
[Cl-].[Cl-].[CH2:3]([C:7]1([Zr+2:13]C2(CCCC)C=CC(C)=C2)[CH:11]=[CH:10][C:9]([CH3:12])=[CH:8]1)[CH2:4][CH2:5][CH3:6].[Li][CH3:25]>C1(C)C=CC=CC=1>[CH3-:3].[CH3-:25].[CH3:6][CH2:5][CH2:4][CH2:3][C-:7]1[CH:8]=[C:9]([CH3:12])[CH:10]=[CH:11]1.[CH3:6][CH2:5][CH2:4][CH2:3][C-:7]1[CH:8]=[C:9]([CH3:12])[CH:10]=[CH:11]1.[Zr+4:13]

Participants

4

Reactant 2

HCID 178418348HCID 178418348, compoundHCID 178442028HCID 178442028, compound

Product 1

HCID 92002078HCID 92002078, compoundYield 87%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

Bis(1-butyl-3-methylcyclopentadienyl)zirconium dichloride (2.71 g, 6.26 mmol)was dissolved in 21.4 g of toluene. Low-halide MeLi (˜1.5 M in ether, 8.0 mL) was added dropwise at ambient temperature. A white solid formed immediately. The reaction was allowed to stir for 1.5 hours. Analysis of the reaction showed 3.5 mol % of mono-methyl intermediate. An additional aliquot of MeLi (0.4 mL) was then added to consume the monomethyl intermediate. After stirring overnight, the supernatant liquid was reanalyzed to verify that the reaction was complete. The slurry was filtered on a medium flit and the solvent was removed in vacuo. A light yellow liquid of bis(1-butyl-3-methyl-cyclopentadienyl)zirconium dimethyl remained (2.13 g, 87% yield).

Workup

  1. additionwas added dropwise at ambient temperature
  2. customA white solid formed immediately
  3. customto consume the monomethyl intermediate
  4. stirringAfter stirring overnight
  5. filtrationThe slurry was filtered on a medium flit
  6. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-413ebdfb7ad24eae9df5848b3a05093a
Source dataset
uspto-grants-2003_05
Patent number
US06562991B1

Reaction notes

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