HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 2-{1-[4-(4-Methoxy-phenyl)-butyl]-1H-imidazol-2-yl}-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2-Methyl-2-butanol | HCID 6405 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(4-Bromobutyl)-4-methoxybenzene | HCID 578191 | — |
| Reactant | 2-(1H-imidazol-2-yl)ethan-1-ol | HCID 15016080 | — |
| Product | 2-{1-[4-(4-Methoxy-phenyl)-butyl]-1H-imidazol-2-yl}-ethanol | HCID 23614536 | — |
Reaction Steps
A mixture of 3.65 g (15.0 mmol) 1-(4-bromo-butyl)-4-methoxy-benzene, 2.52 g (22.5 mmol) 2-(1H-imidazol-2-yl)-ethanol, 2.74 g (16.5 mmol) potassium iodide, 0.90 g (22.5 mmol) sodium hydroxide and 15 ml 2-methyl-2-butanol was heated to reflux for 12 h. Solvents were distilled off, the residue dissolved in toluene and washed with water. After drying over Na2SO4 and removal of solvents in vacuo the residue was stirred with 7 ml ethyl acetate, isolated by filtration, washed with ethyl acetate and dried. Yield 2.41 g (59%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235574B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-d4f0dd5d70c74ffaa5fbb4bd293f7e3e |
| Source note | uspto-grants-2007_06 |