Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][CH2:11]Cl)=[CH:4][CH:3]=1.[CH3:13][N:14]1[CH:18]=[CH:17][N:16]=[CH:15]1>>[Cl-:1].[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][CH2:11][N+:16]2[CH:17]=[CH:18][N:14]([CH3:13])[CH:15]=2)=[CH:4][CH:3]=1Participants
3
Procedure
Combine 6.1 g (0.03 mole) 1-chloro-4-(4-chlorobutyl)benzene with 2.5 g (0.03 mole) 1-methyl-1H-imidazole and heat at 120° C., following the course of the reaction by thin-layer chromatography on silica gel (methanol: 1M sodium chloride, 95:5). At the completion of the reaction, cool and triturate with ether, collect the solid and recrystallize from 50 ml hot acetone to obtain the title compound.
Workup
- customthe course of the reaction by thin-layer chromatography on silica gel (methanol: 1M sodium chloride, 95:5)
- customAt the completion of the reaction
- temperaturecool
- customtriturate with ether
- customcollect the solid
- customrecrystallize from 50 ml hot acetone
Sources & evidence
- ORD record
- ord-789f015a518643958156a7ed367e7d7e
- Source dataset
- uspto-grants-1986_09
- Patent number
- US04613609
Linked notes
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