HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 5-Carboxy-5,5-dimethylpentyltriphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 10036524 | HCID 10036524 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Carboxy-5,5-dimethylpentyltriphenylphosphonium bromide | HCID 86108623 | 58.2% |
Reaction Steps
6-Bromo-2,2-dimethylhexanoic acid (3.8 g, 17 mmole) and triphenylphosphine (4.9 g, 18.7 mmole) were dissolved in acetonitrile (30 ml), and the solution was heated under reflux for 20 hours. After the completion of the reaction, the solvent was removed under reduced pressure, and the residue was treated with toluene, followed by thorough stirring. The insolubles were seperated from the toluene solution, and crystallized from ethyl acetate to give 5-carboxy-5,5-dimethylpentyltriphenylphosphonium bromide (4.8 g, 58%) [NMR (δ value): 1.10 (6H,s), 1.4-1.6 (6H), 3.4-3.8 (2H)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04518602 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-235270cfcd6843f9990fd14a6abeacb6 |
| Source note | uspto-grants-1985_05 |