Tetrahydrofuran → 4-[1-(1-Imidazolyl)-butyl]-benzophenone
Reaction equation
[N:1]1([CH:6]([C:10]2[CH:17]=[CH:16][C:13]([C:14]#N)=[CH:12][CH:11]=2)[CH2:7][CH2:8][CH3:9])[CH:5]=[CH:4][N:3]=[CH:2]1.[C:18]1([Mg]Br)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.[O:26]1CCCC1>>[N:1]1([CH:6]([C:10]2[CH:17]=[CH:16][C:13]([C:14]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[O:26])=[CH:12][CH:11]=2)[CH2:7][CH2:8][CH3:9])[CH:5]=[CH:4][N:3]=[CH:2]1Participants
4
Procedure
The 4-[1-(1-imidazolyl)-butyl]-benzonitrile is reacted with phenylmagnesium bromide under standard conditions analogously to example 11 in tetrahydrofuran. 0.83 g of 4-[1-(1-imidazolyl)-butyl]-benzophenone with a boiling point of 175° C./0.03 mbar is obtained.
Sources & evidence
- ORD record
- ord-a59209496495444088583fc45593208a
- Source dataset
- uspto-grants-1991_09
- Patent number
- US05045558
Reaction notes
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