HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → (4-Carboxybutyl)triphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-Bromovaleric acid | HCID 16368 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (4-Carboxybutyl)triphenylphosphonium bromide | HCID 161236 | 87% |
Reaction Steps
A mixture of 5-bromopentanoic acid (6.9 g, 38 mmol) and triphenylphosphine (10 g, 38 mmol) in dry acetonitrile (30 ml) was heated under reflux overnight. Evaporation of solvent yielded crystals. The resultant crystals were washed with a small amount of acetonitrile and dried at room temperature under reduced pressure to afford a target product, (4-carboxybutyl)-triphenylphosphonium bromide (14.6 g, 87%), which was used in the next step without any further treatment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06642250B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-d3f90a85cbc14dbe8b2ea5eb42b4ea5e |
| Source note | uspto-grants-2003_11 |