HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → (4-Phenylbutyl)triphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Bromo-4-phenylbutane | HCID 259668 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (4-Phenylbutyl)triphenylphosphonium bromide | HCID 18187515 | — |
Reaction Steps
A solution of 4-phenylbutyl bromide from the Step A (24.7 g) and triphenylphosphine (19.00 g) in toluene (100 mL) was heated at 120-130° C. for 3 days. The reaction was cooled to rt and the solid precipitate was collected by filtration, washed with toluene and air dried. The solid was dissolved in a 2:1 mixture of water and acetonitrile and gave the title compound (30.6 g) as a white solid after lyopholization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06358979B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-762cfd9886714d4db5bb3ab9492faa00 |
| Source note | uspto-grants-2002_03 |