HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester | HCID 70670 | 80.4% |
Reaction Steps
To a solution of triphenylphosphine (26.20 g, 100 mmol) in benzene (150 ml) was added ethyl bromoacetate (16.70 g, 100 mmol) at 0-5° C. The mixture was kept at room temperature for 16 h. The resulting phosphonium salt was filtered, washed with benzene (100 ml), and dried. To a solution of the solid in water (200 ml) was added benzene (200 ml), followed by 10% NaOH solution (100 ml). The organic layer was separated, and the aqueous layer was extracted with benzene (200 ml). The combined organic layers were washed with water (100 ml) and brine (100 ml), concentrated to 50 ml in vacuo, and poured onto hexane (200 ml). The precipitate was filtered and dried to afford the desired phosphorane (28.00 g, 80%) as a colorless solid. mp 128-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06906205B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-e63471406a3d44649f40958bfb97e7d7 |
| Source note | uspto-grants-2005_06 |