HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → 2-chloro-1H-benzo[d]imidazol-5-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-Chloro-5-methoxy-1H-benzimidazole | HCID 519197 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-chloro-1H-benzo[d]imidazol-5-ol | HCID 22030958 | 159.1% |
Reaction Steps
2-Chloro-5-methoxybenzimidazole (0.3 g, 1.64 mmol) was suspended in dichloromethane (20 ml) under argon followed by the addition of boron tribromide (233 ul, 2.46 mmol). The reaction mixture was stirred for 2 hours at ambient temperature. The solvent was evaporated and the resulting powder was added in portions to methanol (30 ml). Silica was added and the solvent was evaporated. The resulting powder was placed on the top of a silica column and the product was eluted off using dichloromethane/methanol (95/5). Evaporation of the solvent and trituration in ether gave 2-chloro-5-hydroxybenzimidazole (440 mg, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492560B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-c6a16ab737e4468b944ce467d07b7152 |
| Source note | uspto-grants-2013_07 |