HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitromethane → (3-Methylisoxazole-5-yl)glyoxal-2-oxim
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 3-Methyl-1,2-oxazole-5-carbaldehyde | HCID 10582758 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (3-Methylisoxazole-5-yl)glyoxal-2-oxim | HCID 88761968 | 70.8% |
Reaction Steps
In 50 ml of ethanol were dissolved 5.5 g of 3-methylisoxazole-5-carbaldehyde and 3.3 g of nitromethane. To the solution was added dropwise a solution of sodium ethoxide in ethanl, which had been prepared from 1.5 g of sodium and 30 ml of ethanol, while stirring at room temperature. After dropping the resultant was stirred for a further 3 hrs. at room temperature and then ether was added thereto to separate the sodium salt. This was dissolved in water, which was followed by acidification with hydrochloric acid. The resulting precipitate was filtered off and recrystallized from chloroform to obtain 5.4 g of (3-methylisoxazole-5-yl)glyoxal-2-oxim having m.p. of 179° C.-180° C. Yield, 70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04224450 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-9c98732d38e645a6be69603cd1e65629 |
| Source note | uspto-grants-1980_09 |