HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Phosphonium, (5-hydroxypentyl)triphenyl-, bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Pentanol, 5-bromo- | HCID 118709 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Phosphonium, (5-hydroxypentyl)triphenyl-, bromide | HCID 2784772 | — |
Reaction Steps
An equivalent of 5-bromopentanol and an equivalent of triphenylphosphine in refluxed ethanol are placed in a flask. After 72 hours of agitation in these conditions, and once returned to ambient temperature, the ethanol is evaporated under vacuum and the residue is placed into toluene at 4° C. overnight. The (5-hydroxypentyl)triphenylphosphonium bromide formed is filtered on a frit, rinsed with methyl tert-butyl ether then dried under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09051531B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-a220f2c9520343af94c86a165878c8c8 |
| Source note | uspto-grants-2015_06 |