HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylphosphine → Ferrocene-1,1'-bis-(diphenylphosphine)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | Acetonitrile tetrahydrofuran | HCID 22177404 | — |
| Reactant | HCID 178506418 | HCID 178506418 | — |
| Catalyst | Iodine | HCID 807 | — |
| Product | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | 94% |
Reaction Steps
100 mg (0.171 mmol) of 1,1′-Bis(diphenyloxyphosphino)ferrocene were treated with I2 4 mg (16 μmol) and tributylphosphine 170 μL (0.68 mmol) in acetonitrile/THF (1:1 v/v) 1 mL. The mixture was stirred at room temperature for 10 minutes under nitrogen atmosphere before it was quenched with H2O (100 μL). The reaction mixture was diluted with ethyl acetate (10 mL) and was washed with portions of sat. NaHCO3 (3×5 mL). The organic fraction was dried with Na2SO4, filtered and the solvent evaporated under vacuum. The resulting residue was recrystallized from ethanol, the resulting crystals were filtered, washed and dried in vacuum, giving 89 mg (0.160 mmol, 94%) of 1,1′-Bis(diphenylphosphino)ferrocene (dppf).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735629B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-ebfca4431dd846daacbfbd844d5a65a7 |
| Source note | uspto-grants-2014_05 |