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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387337Generated: October 31, 2026

Acetic Acid → HCID 53806169, compound

https://huagongshe.com/reaction/1387337

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 numberUS06268312B1
Source datasetuspto-grants-2001_07
ORD IDord-a5e02afcb3ac44f7a15091691854cfc7
Source noteuspto-grants-2001_07