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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342182Generated: October 29, 2026

Methanol → 2-(2-hydroxymethylphenyl)-2-methoxyimino-N-methylacetamide

https://huagongshe.com/reaction/342182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactant2-[2-{(1-ethoxyethyl)oxymethyl}phenyl]-2-methoxyimino-N-methylacetamideHCID 53674405—
SolventSodium chloride; waterHCID 57417360—
Product2-(2-hydroxymethylphenyl)-2-methoxyimino-N-methylacetamideHCID 5447256090%

Reaction Steps

Methanol (4 ml) and pyridinium p-toluenesulfonate (0.04 g, 0.00017 mol) were added to an E/Z mixture of 2-[2-{(1-ethoxyethyl)oxymethyl}phenyl]-2-methoxyimino-N-methylacetamide (0.50 g, 0.0017 mol), and the mixture was stirred under reflux for 2 hours. After completion of the reaction, half-saturated brine (100 ml) was added, and the mixture was extracted with dichloromethane (50 ml) twice. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (ethyl acetate/n-hexane) to obtain 2-(2-hydroxymethylphenyl)-2-methoxyimino-N-methylacetamide (0.34 g, Yield: 90.0%, E/Z=96/4) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856573
Source datasetuspto-grants-1999_01
ORD IDord-125ffc03e32f4c31badab379434a35ee
Source noteuspto-grants-1999_01