HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 5-Nitro-2-(pyrrol-1-yl)benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-Nitro-2-(pyrrol-1-yl)benzyl alcohol | HCID 44614021 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Nitro-2-(pyrrol-1-yl)benzyl bromide | HCID 18474002 | 47% |
Reaction Steps
To a solution in dichloromethane (10 ml) of the compound (239 mg) obtained in Example 1b, triphenyl phosphine (345 mg) and carbon tetrabromide (436 mg) were sequentially added dropwise under cooling with ice. The reaction mixture was stirred for 2 hours under cooling with ice and then concentrated at reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent; ethyl acetate:n-hexane=1:9) to give the titled compound (yield,47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06414005B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-a41b09a814d743549544769fdba8ef2f |
| Source note | uspto-grants-2002_07 |