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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427995Generated: October 30, 2026

Potassium Carbonate → methoxy-N-methylphenylacetamide

https://huagongshe.com/reaction/427995

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—
Productmethoxy-N-methylphenylacetamideHCID 15642519178.6%
Product2-[2-[[(E)-benzylideneamino]oxymethyl]phenyl]-2-methoxy-N-methylacetamideHCID 76334241—

Reaction Steps

A solution of 2-hydroxymethyl-α-methoxy-N-methylphenylacetamide (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-(-methoxy-N-methylphenylacetamide (0.32 g, 51%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313150B1
Source datasetuspto-grants-2001_11
ORD IDord-ee08d941b3f94db9ae59d6921eb86cea
Source noteuspto-grants-2001_11