反应 #1458414

ord-0cfc34e8472b4625acb616697f40a1d3

反应方程式

O=C1C(c2ccccc2)=C(c2ccccc2)C(c2ccccc2)=C1c1ccccc1
tetraphenylcyclopentadienone
CC(C)CN
isobutylamine
CCOCC
diethyl ether
CC(C)CN=C1C(c2ccccc2)=C(c2ccccc2)C(c2ccccc2)=C1c1ccccc1
title compound
收率 67.1%
CC(C)CN=C1C(c2ccccc2)=C(c2ccccc2)C(c2ccccc2)=C1c1ccccc1
N-isobutyl-2,3,4,5-tetraphenylcyclopentadieneimine
收率 67.1%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他at 0° C
  2. 2
    温度refluxed for 12 hours
  3. 3
    温度The reaction mixture was cooled
  4. 4
    其他solid precipitation
  5. 5
    过滤The resultant solid was filtered
  6. 6
    其他dried

实验过程

3 g (7.8 mmol) of tetraphenylcyclopentadienone and 3.49 ml (35.1 mmol) of isobutylamine were dissolved in 50 ml of toluene and 0.7 ml (5.85 mmol) of TiCl4 was added thereto at 0° C. The resulting mixture was agitated for 30 minutes at room temperature and then refluxed for 12 hours. The reaction mixture was cooled and diethyl ether was added thereto to induce solid precipitation. The resultant solid was filtered and dried to obtain 2.3 g of the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07156731B2uspto-grants-2007_01