1-Isopropyl-2-methylimidazoline → 1H-Imidazole, 2-methyl-1-(1-methylethyl)-
Reaction equation
[CH:1]([N:4]1[CH2:8][CH2:7][N:6]=[C:5]1[CH3:9])([CH3:3])[CH3:2]>[Ni]>[CH:1]([N:4]1[CH:8]=[CH:7][N:6]=[C:5]1[CH3:9])([CH3:3])[CH3:2]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The procedure of Example 1 was followed except that 40 g of 1-isopropyl-2-methylimidazoline and 5 g of Raney nickel were charged. GLC analysis showed that an 84% yield of 1-isopropyl-2-methyl imidazole was obtained with 98% conversion of imidazoline.
Workup
- additionwere charged
Sources & evidence
- ORD record
- ord-dc9bfd9f3b5846a1a793cbcac7b61afc
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04927942
Reaction notes
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