HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylphosphine → 4-Methoxybiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylphosphine | HCID 68983 | — |
| Reactant | HCID 10856767 | HCID 10856767 | — |
| Catalyst | Nickel | HCID 935 | — |
| Catalyst | Nickel(II) acetylacetonate | HCID 9834912 | — |
| Product | 4-Methoxybiphenyl | HCID 11943 | 1,600% |
Reaction Steps
The procedure was identical to Example 1, with the exception that the nickel catalyst used was derived in situ from a combination of anhydrous nickel acetylacetonate (0.026 g; 5 mol %) and trimethylphosphine (0.20 mL of 1 M solution in toluene; 10 mol %). GC analysis of the organic phase of the hydrolyzed reaction sample after 2 h at 60° C. showed the presence of 1.76 mmol (88% yield) of 4-phenylanisole, 0.11 mmol of 4-methoxybenzophenone imine, and no remaining 4-methoxybenzonitrile in the reaction mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07507830B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-e718b5c472454dc0b21020ceafb9ad37 |
| Source note | uspto-grants-2009_03 |