Reaction #470391

ord-b99acdb60f3f4cef8075d2903a148c0e

Reaction equation

c1ccc(-c2nc3ccccc3[nH]2)cc1
2-phenyl-1H-benzo[d]imidazole
CCO
ethanol
CC(C)c1ccccc1-n1c(-c2ccccc2)nc2ccccc21
desired product
CC(C)c1ccccc1-n1c(-c2ccccc2)nc2ccccc21
1-(2-isopropylphenyl)-2-phenyl-1H-benzo[d]imidazole

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureThe mixture was heated up
  2. 2
    Temperatureto reflux for 24 hours
  3. 3
    Filtrationthe precipitate was collected by filtration
  4. 4
    OtherThe product was purified by column chromatography

Procedure

Intermediate 1 (1.5 g, 2.1 mmol) and 142-isopropylphenyl)-2-phenyl-1H-benzo[d]imidazole (2 g, 6.4 mmol) were mixed with 30 ml of ethanol in a three-neck flask under nitrogen. The mixture was heated up to reflux for 24 hours. After cooled to room temperature, the precipitate was collected by filtration. The product was purified by column chromatography using 1:2 dichloromethane and hexanes as eluent. 0.7 g of desired product was obtained after purification.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08367223B2uspto-grants-2013_02