Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226215Generated: October 31, 2026

Water → (S)-2-((S)-1-azido-2-phenylethyl)oxirane

https://huagongshe.com/reaction/226215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Nitro-benzenesulfonic acid 3-azido-2-hydroxy-4-phenyl-butyl esterHCID 86616463—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product(S)-2-((S)-1-azido-2-phenylethyl)oxiraneHCID 1095432095.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557137B2
Source datasetuspto-grants-2009_07
ORD IDord-c09807d698b64033ad747bd812e792fa
Source noteuspto-grants-2009_07