Reacción #806265

ord-948f7e175640492b98f7c9a38557aeb4

Ecuación de reacción

C[SiH](C)[Zr+2]([CH]1CCC2CC=CC=C21)[CH]1CCC2CC=CC=C21.[Cl-].[Cl-]
rac-dimethylsilyl-bis (tetrahydroindenyl) zirconium dichloride
CCC[CH2][Sn]([F])([CH2]CCC)[CH2]CCC
tributyltin fluoride
C[SiH](C)[Zr+2]([CH]1CCC2CC=CC=C21)[CH]1CCC2CC=CC=C21.[F-].[F-]
rac-dimethylsilylbis (tetrahydroindenyl) zirconium difluoride

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónwas then filtered
  2. 2
    Otroto give a straw-yellow solution
  3. 3
    OtroThe solution was then evaporated in vacuo
  4. 4
    Otroleaving a manila-colored, thick suspension
  5. 5
    LavadoThe suspension was washed with pentane (20 mL
  6. 6
    Otro3×5 mL) to give a white, micro crystalline solid
  7. 7
    OtroThe solid was dried in vacuo
  8. 8
    Otroto yield 0.76 g (82%)

Procedimiento

To a murky green-yellow solution of rac-dimethylsilyl-bis (tetrahydroindenyl) zirconium dichloride [DMS bis (THI) ZrCl2] (1.00 g, 2.19 mmol, 1.00 eq.) in dichloromethane (15 mL) was added tributyltin fluoride (1.42 g, 4.59 mmol, 2.10 eq.). The reaction lightened immediately. The reaction was stirred for one hour and was then filtered to give a straw-yellow solution and a small amount of brownish solid. The solution was then evaporated in vacuo, leaving a manila-colored, thick suspension. The suspension was washed with pentane (20 mL, then 3×5 mL) to give a white, micro crystalline solid. The solid was dried in vacuo to yield 0.76 g (82%). 1H NMR (CD2Cl2): δ 0.80 (s, 6H, SiMe2, 1.45–1.9 and 2.4–2.7 (br m, 16H, aliphatic-ring-H), 5.61 (d, 2H, cyclopentadienyl-ring-H), 6.27 (br s, 2H, cyclopentadienyl-ring-H). 19F NMR (CD2Cl2): δ 19.9 (s).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07132382B2uspto-grants-2006_11