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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617392Generated: October 30, 2026

Potassium Carbonate → 2-[2-[[(E)-benzylideneamino]oxymethyl]phenyl]-2-methoxy-N-methylacetamide

https://huagongshe.com/reaction/617392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(Z)-Benzaldehyde oximeHCID 12143—
ReactantThionyl ChlorideHCID 24386—
Reactant2-hydroxymethyl-alpha-methoxy-N-methyl-phenylacetamideHCID 70239316—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product2-[2-[[(E)-benzylideneamino]oxymethyl]phenyl]-2-methoxy-N-methylacetamideHCID 7633424151.2%

Reaction Steps

A solution of 2-hydroxymethyl-α-methoxy-N-methyl-phenylacetamide (0.42 g, 2.0 mmol) in tetrahydrofuran (4 ml) was stirred at 0° C., and thionyl chloride (0.17 ml, 2.4 mmol) and one drop of N,N-dimethylformamide were added. The mixture was stirred at room temperature for 2 hours, and water was added. The resulting mixture was extracted with ether, washed with saturated brine and dried over anhydrous magnesium sulfate. Evaporation of the solvent gave a crude product (0.38 g) as an oil. Benzaldehyde oxime (0.37 g, 3.1 mmol) and potassium carbonate (0.55 g, 4.0 mmol) were added to a solution of the crude product in N,N-dimethylformamide (6 ml), and the mixture was stirred at room temperature for 3 days. Water was added, and the mixture was extracted with ether and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by column chromatography on silica gel (n-hexane/ethyl acetate=13/7) to give the desired compound (E)-2-benzylideneaminooxymethyl-α-methoxy-N-methylphenylacetamide (0.32 g, 51%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948819
Source datasetuspto-grants-1999_09
ORD IDord-0d04b4f7c7cc4ee9878b3d0245a44f62
Source noteuspto-grants-1999_09