반응 #468424

ord-e0a2b81579b5495ba5ae92607d42549a

반응 방정식

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

반응 조건

온도
-30°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출the remaining powder was extracted with CH2Cl2
  2. 2
    기타Centrifugation afforded

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06306791B2uspto-grants-2001_10