HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 2-(6-bromoheptyl)-1H-benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(6-hydroxyheptyl)-1H-benzimidazole | HCID 22643411 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(6-bromoheptyl)-1H-benzimidazole | HCID 22643429 | 75.8% |
Reaction Steps
2.18 g of the compound obtained in Example 19a, 4.97g of carbon tetrabromide and 3.93 g of triphenylphosphine were added to 30 ml of tetrahydrofuran and the mixture was reacted overnight at room temperature. After the reaction was completed, the solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:1) to obtain 2.10 g of the title compound as pale yellow solid (yield: 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06815455B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-caf644fbcd154e109d938944ddf8b008 |
| Source note | uspto-grants-2004_11 |