HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (S)-2-((S)-1-azido-2-phenylethyl)oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3(S)-azido-4-phenyl-1-(p-toluenesulphonyloxy)-2(S)-butanol | HCID 11760204 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-2-((S)-1-azido-2-phenylethyl)oxirane | HCID 10954320 | 65.4% |
Reaction Steps
A solution of 280 mg (5 mmol) of potassium hydroxide in 10 ml of ethanol were added to a solution of 1.37 g (3.8 mmol) of 3(S)-azido-4-phenyl-1-(p-toluenesulphonyloxy)-2(S)-butanol in 50 ml of ethanol and the mixture was stirred at room temperature for 1 hour. The mixture was then evaporated to dryness and the residue was partitioned between water and dichloromethane. The aqueous phase was back-extracted twice with dichloromethane. The organic phases were combined, dried over anhydrous magnesium sulphate and evaporated to give an oil which was purified by flash chromatography on silica gel using n-hexane/ethyl acetate (4:1) for the elution. There was obtained 0.47 g of 2(S)-[1(S)-azido-2-phenylethyl]oxirane: MS: m/e 189 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05488115 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-a6182bc642aa43f68b34f1ec858eb6a0 |
| Source note | uspto-grants-1996_01 |