HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 57764525, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | HCID 57764505 | HCID 57764505 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexamethyldisilazane | HCID 13838 | — |
| Product | HCID 57764525 | HCID 57764525 | 310% |
Reaction Steps
The compound from Step A (112 mg, 0.3 mmol) was heated at reflux in hexamethyldisilazane (15 mL) for 16 hours. The mixture was evaporated to dryness to give a syrup which was dissolved in dry THF (12 mL). PPh3 (10 mg; 0.04 mmol), PdCl2 (3.5 mg; 0.02 mmol) and AlMe3 (100 μl; 0.94 mmol) were added. The mixture was reflux for 5 hours. The mixture was evaporated to dryness. The crude product was dissolved in methanol (30 mL) in the presence of ammonium chloride. The mixture was evaporated to dryness and the residue was purified on silica gel reverse-phase (C18) using water/acetonitrile (from 9/1 to 6/4) as eluant to give the title compound (35 mg) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09186369B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-6621c3c1daa24d7f9f1bf50a96529aa4 |
| Source note | uspto-grants-2015_11 |