HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylorthoformate → 2-(2,5-dimethylphenoxymethyl)phenyl 1,3,4-oxadiazol-2-yl ketone O-methyloxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylorthoformate | HCID 53630039 | — |
| Reactant | 2-(2,5-Dimethylphenoxymethyl)-alpha-methoxyiminophenylacetohydrazide | HCID 86584675 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2,5-dimethylphenoxymethyl)phenyl 1,3,4-oxadiazol-2-yl ketone O-methyloxime | HCID 54213659 | 19.8% |
Reaction Steps
Ethyl orthoformate (2 ml) was added to 2-(2,5-dimethylphenoxymethyl)-α-methoxyiminophenylacetohydrazide (0.49 g, 1.5 mmol), and the mixture was stirred under reflux for 4 hours. After completion of the reaction, water (100 ml) was added, and the mixture was extracted with dichloromethane. The dichloromethane layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate/n-hexane to give 2-(2,5-dimethylphenoxymethyl)phenyl 1,3,4-oxadiazol-2-yl ketone O-methyloxime (0.10 g, 19.8%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06362212B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-1fb2cea9cd2042dd96ce484c6e97769f |
| Source note | uspto-grants-2002_03 |