反应 #470394
ord-a3a8d3c2613447acba254d6162d7c5c4
反应方程式
N1-(2,6-diisopropylphenyl)benzene-1,2-diamine
→
desired product
收率 59.9%
1-(2,6-diisopropylphenyl)-2-phenyl-1H-benzo[d]imidazole
收率 59.9%
反应条件
详细条件
See reaction.notes.procedure_details.
后处理
- 1温度under reflux for 3 hours
- 2温度The reaction mixture was heated up again
- 3温度to reflux overnight
- 4其他Air was bubbled through the reaction
- 5温度while reflux
- 6其他The solvent was evaporated
- 7workup.DISSOLUTIONThe residue was dissolved in dichloromethane (200 mL)
- 8其他The crude product was purified by column chromatography
实验过程
N1-(2,6-diisopropylphenyl)benzene-1,2-diamine (8.5 g, 32 mmol) and benzldehyde (3 g, 28.8 mmol) were reacted in acetonitrile (100 ml) under reflux for 3 hours. The reaction mixture was cooled to room temperature. Ferric chloride (0.05 g, 0.28 mmol) was added. The reaction mixture was heated up again to reflux overnight. Air was bubbled through the reaction while reflux. The solvent was evaporated. The residue was dissolved in dichloromethane (200 mL) and ran through a short silica gel plug. The crude product was purified by column chromatography using dichloromethane to 3% of ethyl acetate in dichloromethane. 3.4 g of desired product was obtained.