Reaktion #468424

ord-e0a2b81579b5495ba5ae92607d42549a

Reaktionsgleichung

Cc1ccccc1
Toluene
[Cl-].[Cl-].[Cl-].[Cl-].[Zr+4]
ZrCl4
Cc1ccccc1
toluene
[Zr+2].c1cc[cH-]c1.c1cc[cH-]c1
zirconocene

Reaktionsbedingungen

Temperatur
-30°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe remaining powder was extracted with CH2Cl2
  2. 2
    SonstigeCentrifugation afforded

Vorschrift

1H NMR (d8-THF): δ 1.4 (d, 12H, Me), 3.22 (s, 4H, bridge CH2), 3.4 (septet, 2H, CHMe2), 5.93 (s, 2H, CH), 6.28 (m, 4H, aromatic CH), 7.08 (t, 2H, aromatic CH), 7.22 (t, 2H, aromatic CH), 7.28 (t, 4H, aromatic CH), 7.66 (d, 4H, aromatic CH) ppm. The dianion was suspended in toluene and cooled to −30° C.; 0.15 g of ZrCl4 (0.64 mmol) were added and the reaction niixture was stirred for 4 hours at 20° C. and then centrifuged. Toluene was discarded and the remaining powder was extracted with CH2Cl2. Centrifugation afforded a mixture of the two isomers rec/meso-1,2-ethylene-bis(1-isopropyl-4-phenyl-2-indenyl)zirconium dichloride, about in a 1:1 ratio.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06306791B2uspto-grants-2001_10