HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1-Benzyl-2-methyl-5-bromo-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1H-Imidazole, 2-methyl-1-(phenylmethyl)- | HCID 83699 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-Benzyl-2-methyl-5-bromo-1H-imidazole | HCID 66868795 | 84.2% |
Reaction Steps
Add N-bromosuccinimide (7.85 g, 44 mmol) to a solution of 1-benzyl-2-methyl-1H-imidazole (8.0 g, 46 mmol) in chloroform (200 mL) and stir for 6 h. Wash with saturated aqueous sodium hydrogen carbonate and saturated aqueous NaCl, dry over MgSO4, and filter through a pad of silica gel. Concentrate filtrate and suspend the residue in diethyl ether (600 mL), heat to reflux, and filter hot. Concentrate ether filtrate to give the title compound as a tan solid (9.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07582652B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-42c98c3babcb49f8bfa577afcb1884f8 |
| Source note | uspto-grants-2009_09 |