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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782034Generated: October 30, 2026

Nitrogen → N-{4-Methoxy-2-[(2S)-oxiran-2-ylmethoxy]phenyl}acetamide

https://huagongshe.com/reaction/1782034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantCesium carbonateHCID 10796—
ReactantBenzenesulfonic acid, 3-nitro-, (2S)-2-oxiranylmethyl esterHCID 146490—
Reactant2'-Hydroxy-4'-methoxyacetanilideHCID 4105139—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-{4-Methoxy-2-[(2S)-oxiran-2-ylmethoxy]phenyl}acetamideHCID 71570340122.2%

Reaction Steps

N-(2-Hydroxy-4-methoxyphenyl)acetamide (18.12 g, 0.1 mol) and (2S)-oxiran-2-ylmethyl 3-nitrobenzenesulfonate (25.92 g, 0.1 mol) were dissolved in dry DMF (75 mL) and stirred under nitrogen (N2) on an ice-bath. Cesium carbonate (35.8 g, 0.11 mol) was added and the stirring under N2 was continued at ambient temperature overnight. The mixture was poured into ethyl acetate (1 L) and water (250 mL). The organic phase was washed with water (3×250 mL), dried over Na2SO4, filtered and concentrated in vacuo to give an orange solid crude product (29 g), which was recrystallized from ethanol (100 mL) and washed with ether to give white crystals. More white crystals were obtained from the mother liquor, after evaporation and recrystillazition from 2-propanol. Total yield 15 g (63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498338B2
Source datasetuspto-grants-2009_03
ORD IDord-1ec6e476ce1f4d9494af31ff61057d6f
Source noteuspto-grants-2009_03