HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (S)-2-((S)-1-azido-2-phenylethyl)oxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Nitro-benzenesulfonic acid 3-azido-2-hydroxy-4-phenyl-butyl ester | HCID 86616463 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-2-((S)-1-azido-2-phenylethyl)oxirane | HCID 10954320 | 95.1% |
Reaction Steps
A solution of 1.0 g (2.5 mmol) of 4-Nitro-benzenesulfonic acid 3-azido-2-hydroxy-4-phenyl-butyl ester (Kick, E. K.; Ellman, J. A. J. Med. Chem. 1995, 38, 1427-30) in 12 mL of Ethanol and 8 mL of ethyl acetate is treated with KOH (157 mg, 2.8 mmol). After 2 h at rt 10 mL of water is added and 20 mL of CH2Cl2 is added. The organic layer is separated, washed with brine and Na2SO4, and concentrated. Chromatography eluting with hexanes/ethyl acetate 5:1 provides 450 mg (95%) of the desired product. 1H NMR (δ) 7.21-7.36 (m, 5H), 3.58 (dt, 2H, J=9, 5 Hz), 3.05 (m, 1H) 2.97 (dd, 1H, J=13.9, 4.8), 2.77-2.83 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07557137B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-c09807d698b64033ad747bd812e792fa |
| Source note | uspto-grants-2009_07 |