HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 4-(1-Bromoethyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-(1-Hydroxyethyl)benzonitrile | HCID 583335 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-(1-Bromoethyl)benzonitrile | HCID 21834637 | — |
Reaction Steps
To a solution of 1-(4-Cyanophenyl)ethanol 1.01 g, 6.84 mmol), in diethyl ether (15 ml) and triphenylphosphine (2.14 g, 8.17 mmol), was added carbon tetrabromide (2.82 g, 8.50 mmol) in dieathylether (20 ml) at room temperature. After 30 min the reaction was filtered through celite and evaporated to dryness. The residue was purified by chromatography (SiO2, 5% EtOAc in hexanes) to afford the title compound as an oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05756528 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-8400164f6e6e4528b670fc56db847540 |
| Source note | uspto-grants-1998_05 |