HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → 1-Butyl-4-dimethoxymethyl-2-phenyl-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Dimethoxymethyl-2-phenyl-1H-imidazole | HCID 178499560 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Butyl-4-dimethoxymethyl-2-phenyl-1H-imidazole | HCID 18437788 | — |
Reaction Steps
A solution of 4-dimethoxymethyl-2-phenyl-1H-imidazole 208 (2.18 g, 10 mmol) and n-butyl bromide (2.74 g, 20 mmol) in anhydrous DMSO (15 mL) is added to a suspension of powdered potassium hydroxide (0.96 mg, 15 mmol) in DMSO (20 mL) at room temperature over 3 h. The mixture is then stirred at rt for 16 h. The mixture is diluted with ether and washed with water (three times), brine, and dried over anhydrous sodium sulfate. Removal of the solvent and purification of the residue affords the desired product. Yield: 2.5 g; LC-MS (MH+): 275.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07186734B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-1e41df7030434fe9adac9bc5e2f614bb |
| Source note | uspto-grants-2007_03 |