1-Methylimidazole → HCID 178490138, compound
Reaction equation
[CH3:1][N:2]1[CH:6]=[CH:5][N:4]=[CH:3]1.[Br:7][CH2:8][CH2:9][CH2:10][C:11]1[CH:16]=[CH:15][C:14]([O:17][CH3:18])=[CH:13][CH:12]=1>>[Br-:7].[CH3:18][O:17][C:14]1[CH:15]=[CH:16][C:11]([CH2:10][CH2:9][CH2:8][N+:4]2[CH:5]=[CH:6][N:2]([CH3:1])[CH:3]=2)=[CH:12][CH:13]=1Participants
3
Conditions
- Temperature
- 140 °C
Procedure
A mixture of 2.50 g (0.03 mole) of 1-methyl-1H-imidazole and 6.9 g (0.03 mole) of 1-(3-bromopropyl)-4-methoxybenzene is heated at 140° C. for 1.5 hours. Follow the progress of the reaction by thin-layer chromatography on silica gel (methanol: 1M sodium chloride, 95:5). At the completion, the cooled reaction product is triturated thoroughly with ether and on drying, provides the title compound.
Workup
- customthe progress of the reaction by thin-layer chromatography on silica gel (methanol: 1M sodium chloride, 95:5)
- customAt the completion, the cooled reaction product
- customis triturated thoroughly with ether
- customon drying
Sources & evidence
- ORD record
- ord-b4506c6b1dc343459d9a01c6adf7bcea
- Source dataset
- uspto-grants-1986_09
- Patent number
- US04613609
Reaction notes
Loading…