HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 22009002, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Allyltributylstannane | HCID 90628 | — |
| Reactant | 3-Bromodiphenyl ether | HCID 96165 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22009002 | HCID 22009002 | — |
Reaction Steps
A suspension of 1-bromo-3-phenoxybenzene (2.01 g; 8.08 mmol), PdCl2(PPh3)2 (296 mg; 0.42 mmol), allyl tributyltin 3.13 g; 9.46 mmol), triphenylphosphine (455 mg; 1.73 mmol) and LiCl (1.39 g; 33 mmol) in 10 ml DMF was stirred at 100° C. for 3 h. After cooling to r.t the mixture was diluted with Et2O (75 ml), washed with water (3×50 ml) and brine, dried over MgSO4 and concentrated. Flash chromatography with hexane afforded the desired material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211197B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-4bfbaf8f9e034294bf609b6228685311 |
| Source note | uspto-grants-2001_04 |