HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-2-Benzhydryloxirane → (2S)-1,1-diphenyl-pent-4-ene-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-2-Benzhydryloxirane | HCID 11789056 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2S)-1,1-diphenyl-pent-4-ene-2-ol | HCID 11390776 | 70.5% |
Reaction Steps
(2R)-2-benzhydryl-oxirane (0.5 g, 2.38 mmol) 23a was dissolved in dry THF (5 ml) and was added into a dry THF solution at −78° C. containing CuI (0.045 g, 0.24 mmol) and vinylmagnesium bromide (5.95 ml of 1.0M solution in THF, 5.95 mmol). The reaction mixture was stirred and allowed to reach room temperature over a period of 2h, and then quenched with saturated NH4Cl solution. The aqueous phase was extracted with ethyl acetate (3×30 ml). The combined organic phase was washed with brine and dried over anhydrous Na2SO4. The solvent was removed and the residue was purified by flash chromatography on silica gel (Hexane/Ethyl Ether=4:1) to give 0.4 g (2S)-1,1-diphenyl-pent-4-ene-2-ol (70%, [α]D=(−)25, c=1, MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915433B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-97f420b978bd400da66a1de4670d2f68 |
| Source note | uspto-grants-2011_03 |