HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-(1-methylimidazol-2-yl)benzylideneamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | N-[(1E)-phenylmethylidene]-1H-imidazol-2-amine | HCID 53795682 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(1-methylimidazol-2-yl)benzylideneamine | HCID 53843952 | 49.9% |
Reaction Steps
N-(2-imidazolyl)benzylideneamine (0.2 g) was dissolved in DMF (4 ml), and potassium t-butoxide (0.15 g) and methyl iodide (0.18 g) were added. The mixture was stirred at room temperature for 3 hours. The solvent was evaporated, and water was added. The mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine and dried over magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography (eluent: chloroform). The resulting crude crystals were recrystallized from diethyl ether--hexane to give the title compound (0.1 g, 49.9%) as pale yellow needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05552427 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-4e1abe74d4f54f24aa0ee8eaf6f59d0b |
| Source note | uspto-grants-1996_09 |