Reaction #806263

ord-40307e589a954b09911c08efff447785

Reaction equation

CCCCC
Pentane
CCC[CH2][Sn]([F])([CH2]CCC)[CH2]CCC
tributyltin fluoride
CCC[C]1([Zr+2][C]2(C)C=C(C)C(C)=C2C)C=CC=C1.[Cl-].[Cl-]
(tetramethylcyclopentadienyl)(propylcyclopentadienyl) zirconium dichloride
CCC[CH2][Sn]([F])([CH2]CCC)[CH2]CCC
tributyltin fluoride
CCC[C]1([Zr+2][C]2(C)C=C(C)C(C)=C2C)C=CC=C1.[F-].[F-]
(tetramethylcyclopentadienyl)(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 0.88 g (96%)

Procedure

To a yellow solution of (tetramethylcyclopentadienyl)(propylcyclopentadienyl) zirconium dichloride [(Me4Cp)(PrCp)ZrCl2] (1.00 g, 2.47 mmol, 1.00 eq.) in dichloromethane (10 mL) was added tributyltin fluoride (1.60 g, 5.18 mmol, 2.09 eq.). The reaction quickly lightened, becoming almost colorless with a small amount of tributyltin fluoride still visible. 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 (15 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 0.88 g (96%). 1H NMR(CD2Cl2): δ 0.92 (t, 3H, CH2CH2CH3), 1.55 (m, 2H, CH2CH2CH3), 1.82 (s, 6H, Me), 1.99 (s, 6H, Me), 2.42 (t, 2H, CH2CH2CH3), 5.93 (s, 1H, ring-H), 5.96 (br m, 2H, ring-H), 6.17 (m, 2H, ring-H). 19F NMR(CD2Cl2): δ 17.5 (s).

Source

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