HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → 3-Butyl-5-(4-methoxy-phenyl)-2-phenyl-3H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178488774 | HCID 178488774 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-Butyl-5-(4-methoxy-phenyl)-2-phenyl-3H-imidazole | HCID 58818033 | — |
Reaction Steps
Potassium hydroxide (4.36, 76 mmol, 1.3 eq.) is suspended in 40 ml of anhydrous DMSO, to the suspension is added a solution 2-phenyl-4-(4-methoxyphenyl)imidazole (15.02, 60 mmol) and bromobutane (8.63 g, 63 mmol, 1.05 eq.) in 80 ml of DMSO at room temperature over 2h, the resulting mixture is stirred over 24h, and then poured into 400 ml of ice-water, extracted with ethyl acetate (100 ml×4), washed,with water and brine, dried over anhydrous sodium sulfate. The solvent is evaporated and the product is purified through flash chromatography to give 16.73 g of 4-({[3-Butyl-5-(4-methoxy-phenyl)-2-phenyl-3H-imidazole. MS (+VE) m/z 307 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119665B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-1104959ac9db496d983a8fb6de416e7d |
| Source note | uspto-grants-2012_02 |