HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-Bromo-7-methoxy-3-methyl-2-trifluoromethylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-Methoxy-3-methyl-2-trifluoromethylbenzimidazole | HCID 18316636 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-Bromo-7-methoxy-3-methyl-2-trifluoromethylbenzimidazole | HCID 18316622 | 92% |
Reaction Steps
To a solution of 7-methoxy-3-methyl-2-trifluoromethylbenzimidazole (1.4 g) in chloroform (50 ml) under nitrogen was added N-bromosuccinimide (1.2 g). The mixture was stirred for 20 minutes before the reaction was quenched by the addition of 5% sodium metabisulphite solution (50 ml) and the organic layer was separated. Washing with water (50 ml), drying over anhydrous magnesium sulphate and removal of the solvent in vacuo gave an orange oil. Purification by flash chromatography eluting with 50% ethyl acetate in hexane gave the title compound as an orange solid (1.73 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353010B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-de379988852f45a1b9e7d4a9df08a5f3 |
| Source note | uspto-grants-2002_03 |