HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Pentafluorobenzyltriphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Pentafluorobenzyl bromide | HCID 74484 | — |
| Product | Pentafluorobenzyltriphenylphosphonium bromide | HCID 87730649 | 90% |
Reaction Steps
A five-liter, three-necked flask equipped with a mechanical stirrer, reflux condenser, and thermometer was charged with toluene (3.3 liters), triphenylphosphine (686 g, 2.62 mole), and pentafluorobenzyl bromide (343 g, 1.31 mole). The contents were stirred and heated slowly to reflux. A white precipitate formed as the reaction progressed. At the completion of the reaction the flask was cooled to ambient temperature and the solid product was filtered and washed with hot toluene (2.6 liters). These solids were dried in a vacuum desiccator to give a 90% yield of pentafluorobenzyltriphenylphosphonium bromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04633020 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-17688f8e310142d09b1573f1989d69f4 |
| Source note | uspto-grants-1986_12 |