Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 178502837 | HCID 178502837 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53806169 | HCID 53806169 | 40.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06268312B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-a5e02afcb3ac44f7a15091691854cfc7 |
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| Source note | uspto-grants-2001_07 |
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