HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → (7-Carboxyheptyl)triphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 8-Bromooctanoic acid | HCID 548275 | — |
| Product | (7-Carboxyheptyl)triphenylphosphonium bromide | HCID 11317723 | 88.5% |
Reaction Steps
Triphenylphosphine (26.3 g) and 8-bromooctanoic acid (21.3 g) were reacted as in Example 82. The crude salt was crystallized from a mixture of ethanol (100 mL), chloroform (200 mL) and ether (500 mL) to give 41 g of (7-carboxyheptyl) triphenylphosphonium bromide, mp 121°-123° C. Anal. Calculated for C26H30BrO2P: C, 64.33; H, 6.23; Br, 16.46. Found: C, 63.97; H, 6.23; Br, 16.07.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04927838 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-17c21f1d935d4bb4b31092deac3f8a2e |
| Source note | uspto-grants-1990_05 |