反応 #1148669

ord-d064166f6363433d86de9fba26f62887

反応方程式

[Li][CH2]CCC
n-Butyllithium
[Cl-].[Cl-].[Cl-].[Cl-].[Zr+4]
Zirconium tetrachloride
CC(C)(C)c1cc(C2=Cc3ccccc3C2)cc(C(C)(C)C)c1
2-(3,5-Di-t-butylphenyl)indene
CC(C)(C)c1cc(C2=Cc3ccccc3[CH]2[Zr+2][CH]2C(c3cc(C(C)(C)C)cc(C(C)(C)C)c3)=Cc3ccccc32)cc(C(C)(C)C)c1.[Cl-].[Cl-]
product
収率 64.0%
CC(C)(C)c1cc(C2=Cc3ccccc3[CH]2[Zr+2][CH]2C(c3cc(C(C)(C)C)cc(C(C)(C)C)c3)=Cc3ccccc32)cc(C(C)(C)C)c1.[Cl-].[Cl-]
Bis(2-(3,5-di-t-butylphenyl)indenyl)zirconium dichloride
収率 64.0%

反応条件

温度
-10°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGThe mixture was then stirred overnight
  2. 2
    その他the solids were collected
  3. 3
    その他the residual solids were removed by filtration through celite
  4. 4
    洗浄The celite was washed with an additional 100 mL of dichloromethane
  5. 5
    その他the solvents were evaporated

実験手順

2-(3,5-Di-t-butylphenyl)indene (13.8 g, 0.045 mol) and anhydrous diethyl ether (250 mL) were placed in a 1 L three-necked flask under argon. n-Butyllithium (28 mL of a 1.6 M solution in hexanes, 0.045 mol) as added over a thirty minute period at 0° C. The solution was stirred for an additional two hours. Zirconium tetrachloride (5.1 g, 0.022 mol), was added incrementally over a one hour period. The mixture was then stirred overnight. The ethereal solution was chilled to −10° C. and the solids were collected. The solids were taken up in 300 mL of dichloromethane and the residual solids were removed by filtration through celite. The celite was washed with an additional 100 mL of dichloromethane, and the solvents were evaporated to give 11.2 g of product (64%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06960550B2uspto-grants-2005_11