HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2S)-2-(4,5-diphenyloxazol-2-yl)oxirane → (4S)-4-(4,5-diphenyloxazol-2-yl)-4-hydroxy-1-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2S)-2-(4,5-diphenyloxazol-2-yl)oxirane | HCID 57131304 | — |
| Reactant | HCID 178461836 | HCID 178461836 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4S)-4-(4,5-diphenyloxazol-2-yl)-4-hydroxy-1-butene | HCID 56991674 | — |
Reaction Steps
To a solution of (2S)-2-(4,5-diphenyloxazol-2-yl)oxirane (12 g) and CuI (0.19 g) in THF (240 ml) was dropwise added a solution of vinylmagnesium chloride in THF (1.0M solution, 101 ml) at −78° C. under N2. The mixture was stirred for 1 hour 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 (4S)-4-(4,5-diphenyloxazol-2-yl)-4-hydroxy-1-butene (9.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06300344B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-525d6f3f68c34670aa445f84667745bc |
| Source note | uspto-grants-2001_10 |