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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411543Generated: October 30, 2026

Diethyl Ether → Benzyl (2s)-2-[(4-cyanophenoxy)methyl]-1-aziridinecarboxylate

https://huagongshe.com/reaction/411543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium HydroxideHCID 14798—
Reactant(1R)-2-{[(Benzyloxy)carbonyl]amino}-1-[(4-cyanophenoxy)methyl]ethyl MethanesulfonateHCID 88118165—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductBenzyl (2s)-2-[(4-cyanophenoxy)methyl]-1-aziridinecarboxylateHCID 9084349769%

Reaction Steps

A solution of NaOH in water (11 mL of 50 wt. %) was added under vigorous stirring to a solution of (1R)-2-{[(benzyloxy)carbonyl]amino}-1-[(4-cyanophenoxy)-methyl]ethyl methanesulfonate (see step (iv) above; 5.7 g, 14.1 mmol) and tetrabutylammonium hydrogensulfate (0.6 g, 1.7 mmol) in DCM (34 mL). The mixture was stirred for 1 h before water (200 mL) and ether (200 mL) were added. The organic phase was washed with water and then dried. The solvents were evaporated and the resulting residue was purified by chromatography (DCM eluant) to yield 3.0 g (69%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559162B2
Source datasetuspto-grants-2003_05
ORD IDord-43e786769e104bee825856b26c727f52
Source noteuspto-grants-2003_05