HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-(2,5-dimethylphenoxymethyl)phenyl oxazol-5-yl ketone O-methyloxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | 2-(2,5-Dimethylphenoxymethyl)-alpha-methoxyiminophenylacetaldehyde | HCID 53861051 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2,5-dimethylphenoxymethyl)phenyl oxazol-5-yl ketone O-methyloxime | HCID 54475482 | 44.6% |
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-methoxyiminophenylacetaldehyde (0.30 g, 1 mmol), and the mixture was 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-dimethylphenoxymethyl)phenyl oxazol-5-yl ketone O-methyloxime (0.15 g, 44.6%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06268312B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-6a473d9db15f4087886b42765bcf57f0 |
| Source note | uspto-grants-2001_07 |