HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 10737216, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 11795253 | HCID 11795253 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10737216 | HCID 10737216 | 97.1% |
Reaction Steps
In 10 ml of a 10% solution of formic acid in tetrahydrofuran (THF), were dissolved 400 mg (1.00 mmol) of 3-(3-allyloxycarbonylbenzenesulfonyl)-1-phenyl-imidazolidin-2,4-dione obtained in Example 33. The resultant solution wad deaerated under reduced pressure. To the solution, 50 mg of tetrakis(triphenylphosphine)palladium and 50 mg of triphenylphosphine were added, followed by stirring at room temperature for 2 hours under shielding from the light. After completion of the reaction, the liquid reaction mixture was concentrated under reduced pressure, and crude crystals obtained as residue were collected by filtration, washed with ethyl acetate and then dried, thereby obtaining 350 mg (yield: 97.0%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05691335 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-00a2fc6b985843e08b192add7dd284e8 |
| Source note | uspto-grants-1997_11 |