1-Methylimidazole → HCID 86655181, compound
Reaction equation
[CH3:1][N:2]1[CH:6]=[CH:5][N:4]=[CH:3]1.[CH3:7][O:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13][Br:14])=[CH:11][CH:10]=1>C1(C)C=CC=CC=1>[Br-:14].[CH3:7][O:8][C:9]1[CH:16]=[CH:15][C:12]([CH2:13][N:4]2[CH:5]=[CH:6][N+:2]([CH3:1])=[CH:3]2)=[CH:11][CH:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Into a 50 ml one-necked flask surmounted by a condenser, there are successively introduced 1 ml (12.5 mmol) of N-methylimidazole, and then 5 g (18.8 mmol) of 4-methoxybenzyl bromide in solution in 25 ml of toluene. The reaction medium is heated under reflux, with stirring, for 2 h 30 min. After cooling to room temperature, the viscous oil formed is separated by decantation and then dried under vacuum at room temperature, 4.65 g of a pale yellow solid are thus obtained whose characteristics are the following:
Workup
- customInto a 50 ml one-necked flask surmounted by a condenser
- temperatureThe reaction medium is heated
- temperatureunder reflux
- customthe viscous oil formed
- customis separated by decantation
- customdried under vacuum at room temperature
Sources & evidence
- ORD record
- ord-7a6363acd9e84fdfaef1dcb5fb9a898e
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08980875B2
Reaction notes
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