反应 #1528391

ord-73acf781ee604fff9ee8aecc97efdfa0

反应方程式

CC(C)c1cccc(C(C)C)c1N1CC(=N)N(c2c(C(C)C)cccc2C(C)C)C1
1,3-bis(2,6-diisopropylphenyl)-iminoimidazoline
[Cl-].[Cl-].[Cl-].[Ti+3][CH]1C=CC=C1
cyclopentadienyltitanium trichloride
CCN(CC)CC
triethylamine
CC(C)c1cccc(C(C)C)c1N1CC(=N)N(c2c(C(C)C)cccc2C(C)C)C1.[Cl-].[Cl-].[Ti+2][CH]1C=CC=C1
1,3-bis(2,6-diisopropylphenyl)-iminoimidazoline cyclopentadienyltitanium dichloride
收率 177.8%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤the thick yellow-orange suspension was filtered
  2. 2
    其他the filtrate evaporated to dryness

实验过程

To a suspension of 1,3-bis(2,6-diisopropylphenyl)-iminoimidazoline (1.02 g, 2.5 mmol) and cyclopentadienyltitanium trichloride (0.55 g, 2.5 mmol) in toluene (20 mL) was added triethylamine (0.4 mL, 4.0 mmol) at ambient temperature. After stirring for 2 hours, the thick yellow-orange suspension was filtered, and the filtrate evaporated to dryness to afford 1.31 g (89% yield) of NMR-pure 1,3-bis(2,6-diisopropylphenyl)-iminoimidazoline cyclopentadienyltitanium dichloride.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07655592B2uspto-grants-2010_02