反応 #831221

ord-558dad95af7248079e9209386a495763

反応方程式

N#CCCCc1cn(C(c2ccccc2)(c2ccccc2)c2ccccc2)cn1
4-(1-(triphenylmethyl)imidazol-4-yl)butanenitrile
[Br][Mg][CH2]CCc1ccccc1
3-phenylpropylmagnesium bromide
CCOCC
diethyl ether
[Cl-].[NH4+]
ammonium chloride
O=C(CCCc1ccccc1)CCCc1c[nH]cn1
1-(1H-Imidazol-4-yl)-7-phenylheptan-4-one

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度to reflux for 6 h
  2. 2
    その他Hydrolysis
  3. 3
    その他the organic phase is separated
  4. 4
    その他for 2 h
  5. 5
    その他The ethanol is removed under vacuum, filtration
  6. 6
    workup.STIRRINGThe title compound is stirred in dichloromethane
  7. 7
    その他recrystallized in the hydrogenmaleate form from ethanol/diethyl ether

実験手順

5 mmol of 4-(1-(triphenylmethyl)imidazol-4-yl)butanenitrile are introduced into a solution of 3-phenylpropylmagnesium bromide in 300 ml of diethyl ether and 100 ml of tetrahydrofuran and the mixture is brought to reflux for 6 h. Hydrolysis is carried out with an ammonium chloride solution, the organic phase is separated and the aqueous phase is stirred with dichloromethane. The combined and concentrated organic phases are brought to boiling point for 2 h in a 2N aqueous/alcohol (ethanol/water) hydrochloric acid solution. The ethanol is removed under vacuum, filtration is carried out and basification is carried out. The title compound is stirred in dichloromethane and recrystallized in the hydrogenmaleate form from ethanol/diethyl ether.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05559113uspto-grants-1996_09