HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Triphenylphosphine Oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 1H-indol-4-ylmethanol | HCID 2773457 | — |
| Reactant | HCID 90234246 | HCID 90234246 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Triphenylphosphine Oxide | HCID 13097 | — |
Reaction Steps
To a solution of 31 (700 mg, 2.83 mmol), (1H-indol-4-yl)methanol (1.25 g, 8.50 mmol), and triphenylphosphine (2.97 g, 11.3 mmol) in tetrahydrofuran (30 mL) at 60° C. under nitrogen atmosphere was added diisopropyl azodicarboxylate (1.43 g, 7.07 mmol). The mixture was cooled to room temperature, concentrated, and purified by chromatography (silica gel, 0-100% ethyl acetate/hexanes) to give crude 59 (1.94 g, contained Ph3PO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09271978B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-c5e09381545241c29db297b8a82e56b5 |
| Source note | uspto-grants-2016_03 |