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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279460Generated: November 2, 2026

Methanol → 2-(2,5-dimethylphenoxymethyl)phenyl oxazol-5-yl ketone O-methyloxime

https://huagongshe.com/reaction/279460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant2-(2,5-Dimethylphenoxymethyl)-alpha-methoxy-iminophenylacetaldehydeHCID 86757907—
SolventDiethyl EtherHCID 3283—
Product2-(2,5-dimethylphenoxymethyl)phenyl oxazol-5-yl ketone O-methyloximeHCID 5447548244.6%

Reaction Steps

p-Toluenesulfonylmethylisocyanide (0.23 g, 1.2 mmol), potassium carbonate (0.18 g, 1.3 mmol) and methanol (2 ml) were added to 2-(2,5-dimethylphenoxymethyl)-α-methoxy-iminophenylacetaldehyde (0.30 g, 1 mmol), and the mixture stirred under reflux for 2 hours. After completion of the reaction, ether (100 ml) was added, and the mixture was washed with brine (80 ml) twice. The ether layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane) and recrystallized from ethyl acetate/n-hexane to give 2-(2,5-dimethylphenoxy-methyl)phenyl oxazol-5-yl ketone O-methyloxime (0.15 g, 44.6%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362212B1
Source datasetuspto-grants-2002_03
ORD IDord-e9c62baa3625482da461529cac07e57b
Source noteuspto-grants-2002_03