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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004360Generated: November 1, 2026

Acetic Acid → HCID 53806169, compound

https://huagongshe.com/reaction/1004360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 178502837HCID 178502837—
SolventDiethyl EtherHCID 3283—
ProductHCID 53806169HCID 5380616940.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

Dioxane (2 ml) and acetic acid (1.5 ml) were added to 2-(4-chlorophenoxymethyl)-N-hydroxyaminomethylene-α-methoxyiminophenylacetamide (0.36 g, 1 mmol), and the mixture was stirred at 120° C. for 4 hours. After completion of the reaction, ether (150 ml) was added, and the mixture was washed with saturated aqueous sodium bicarbonate solution (100 ml) twice. The ether layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate/n-hexane) and recrystallized from ethyl acetate/n-hexane to give 2-(4-chlorophenoxymethyl)phenyl 1,2,4-oxadiazol-5-yl ketone O-methyloxime (0.14 g, 40.8%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048885
Source datasetuspto-grants-2000_04
ORD IDord-0428f8fb3bab4ecca93a2da6c8580e8a
Source noteuspto-grants-2000_04