HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5-bromo-2-butyl-1H-imidazole-4-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (2-butyl-1H-imidazole-4,5-diyl)dimethanol | HCID 15338146 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-bromo-2-butyl-1H-imidazole-4-methanol | HCID 9991571 | — |
Reaction Steps
3.56 Grams (20 mmol) of the N-bromosuccinimide was added to a solution consisting of 3.68 g (20.0 mmol) of the 2-butyl-4,5-bis(hydroxymethyl) imidazole, 40 ml of ethanol and 15 ml of dioxane maintained at a temperature of 45° to 50° C. with stirring. The mixture was further reacted at the same temperature for 30 minutes with stirring, and then the solvent was distilled off under reduced pressure. The obtained reaction product was washed with water and was recrystallized from acetonitrile to obtain a pale yellowish scale-like crystalline 2-butyl-4-bromo-5-(hydroxymethyl) imidazole in an amount of 2.36 g (yield, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05514811 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-025b73636d7a460a9c2331cb9ff512a5 |
| Source note | uspto-grants-1996_05 |