Reaction #806264

ord-a47443a3afa24c9d90c385c0cb0e18dd

Reaction equation

CCCCC
Pentane
CCC[C]1([Zr+2][C]2(CCC)C=CC=C2)C=CC=C1.[Cl-].[Cl-]
bis(propylcyclopentadienyl) zirconium dichloride
CCC[CH2][Sn]([F])([CH2]CCC)[CH2]CCC
tributyltin fluoride
CCC[C]1([Zr+2][C]2(CCC)C=CC=C2)C=CC=C1.[F-].[F-]
bis(propylcyclopentadienyl)zirconium difluoride

Conditions

Temperature
-35°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherThe reaction
  2. 2
    Filtrationwas then filtered
  3. 3
    Otherto give a colorless solution
  4. 4
    OtherThe solution was evaporated in vacuo
  5. 5
    Otherleaving a damp, white solid
  6. 6
    FiltrationThe mixture was filtered
  7. 7
    Otherresulting white solid
  8. 8
    Washwas washed with pentane (3×3 mL)
  9. 9
    Temperaturecooled to −35° C
  10. 10
    OtherThe white solid was dried in vacuo
  11. 11
    Otherto yield 0.75 g (82%)

Procedure

To a straw yellow solution of bis(propylcyclopentadienyl) zirconium dichloride [(PrCp)2ZrCl2] (1.00 g, 2.66 mmol, 1.00 eq.) in dichloromethane (10 mL) was added tributyltin fluoride (1.72 g, 5.57 mmol, 2.10 eq.). The reaction rapidly lightened, turning almost colorless. The reaction was stirred 1 h and was then filtered to give a colorless solution and a small amount of white solid. The solution was evaporated in vacuo, leaving a damp, white solid. Pentane (10 mL) was added and the mixture was cooled to −35° C. The mixture was filtered, and resulting white solid was washed with pentane (3×3 mL) cooled to −35° C. The white solid was dried in vacuo to yield 0.75 g (82%). 1H NMR(CD2Cl2): δ 0.92 (t, 6H, CH2CH2CH3), 1.56 (m, 4H, CH2CH2CH3), 2.44 (t, 4H, CH2CH2CH3), 6.05 (m, 4H, ring-H), 6.30 (m, 4H, ring-H). 19F NMR(CD2Cl2): δ 20.4 (s).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07132382B2uspto-grants-2006_11