HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 2-Benzyloxycarbonylamino-1-phenyl-3,4-epoxy-butane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Benzyloxycarbonylamino-1-phenyl-3-butene | HCID 13606586 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Benzyloxycarbonylamino-1-phenyl-3,4-epoxy-butane | HCID 14887243 | — |
Reaction Steps
To a stirred solution of 2-benzyloxycarbonylamino-1-phenyl-3-butene (1.43 g, 5.08 mmoles) in 20 mL of CH2Cl2 was added 3-chloroperoxybenzoic acid (2.19 g, 60%, 7.62 mmoles) in several portions, and the mixture was stirred at room temperature for 30 hrs. After addition of EtOAc (60 mL), the mixture was washed with saturated NaHCO3 and brine, and the organic layer was dried over Na2SO4. Evaporation of the solvent afforded an oily residue. The crude product was purified by column chromatography on silica gel with elution by 2:8 EtOAc-hexane to give pure 2-benzyloxycarbonylamino-1-phenyl-3,4-epoxy-butane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06525069B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-e6243a691e6e4984bdeb2a535efccdfc |
| Source note | uspto-grants-2003_02 |