Methyl iodide → HCID 88282627, compound
Reaction equation
[OH:1][N:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH2:10][C:11]([OH:13])=[O:12].IC.[C:16](=O)([O-])[O-].[K+].[K+].C([N+](CC)(CC)CC1C=CC=CC=1)C>C(#N)C>[CH3:16][O:1]/[N:2]=[CH:3]/[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[CH2:10][C:11]([OH:13])=[O:12]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
1.8 g (10 mmoles) of 2-hydroxyiminomethyl-phenylacetic acid are reacted with 1.50 ml of iodomethane, 5 g of potassium carbonate and 10 mg of triethylbenzylammonium (TEBA) chloride in 20 ml of anhydrous acetonitrile. The system is left for 6 hours at +80° C. and overnight at ambient temperature.
Sources & evidence
- ORD record
- ord-c735d32531ef4eea82c7e2c516d65b43
- Source dataset
- uspto-grants-1996_11
- Patent number
- US05574153
Reaction notes
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