HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → (3-(1,3-Dioxoisoindolin-2-yl)propyl)triphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-3-Bromopropylphthalimide | HCID 21611 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (3-(1,3-Dioxoisoindolin-2-yl)propyl)triphenylphosphonium bromide | HCID 22018487 | 36.2% |
Reaction Steps
A solution of N-(3-bromopropyl)phthalimide (25.0 g, 93.2 mmol) and triphenylphosphine (24.5 g, 93.2 mmol) in toluene (200 mL) was stirred and heated to reflux for 15 hours. The reaction mixture was cooled to ambient temperature and the resulting precipitate was collected by filtration, washed with toluene, and dried under vacuum to afford (3-(1,3-dioxoisoindolin-2-yl)propyl)triphenylphosphonium bromide as a white powder (17.9 g, 36% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716498B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-ed1f28386bfe44bfaa095c331440ff0a |
| Source note | uspto-grants-2014_05 |