Reacción #1458414

ord-0cfc34e8472b4625acb616697f40a1d3

Ecuación de reacción

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
Rendimiento 67.1%
CC(C)CN=C1C(c2ccccc2)=C(c2ccccc2)C(c2ccccc2)=C1c1ccccc1
N-isobutyl-2,3,4,5-tetraphenylcyclopentadieneimine
Rendimiento 67.1%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroat 0° C
  2. 2
    Temperaturarefluxed for 12 hours
  3. 3
    TemperaturaThe reaction mixture was cooled
  4. 4
    Otrosolid precipitation
  5. 5
    FiltraciónThe resultant solid was filtered
  6. 6
    Otrodried

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07156731B2uspto-grants-2007_01