HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalimide → (4R)-4-(4,5-diphenyloxazol-2-yl)-4-phthalimido-1-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (4S)-4-(4,5-diphenyloxazol-2-yl)-4-hydroxy-1-butene | HCID 56991674 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4R)-4-(4,5-diphenyloxazol-2-yl)-4-phthalimido-1-butene | HCID 54558309 | 73.1% |
Reaction Steps
To a solution of (4S)-4-(4,5-diphenyloxazol-2-yl)-4-hydroxy-1-butene (9.2 g) in THF (100 ml) were added phthalimide (7.0 g) and triphenylphosphine (12.5 g) and diethyl azodiformate (7.5 ml) at room temperature. The mixture was stirred for 2 hours at room temperature and partitioned between ethyl acetate and water. The organic layer was washed with 1N-HCl, water, sat. NaHCO3 and brine. The dried solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel to give (4R)-4-(4,5-diphenyloxazol-2-yl)-4-phthalimido-1-butene (9.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06300344B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-97ba460a673340e3b106d8b58027faaa |
| Source note | uspto-grants-2001_10 |