HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → (E)-4-ethyl-2-methoxyimino-5-nitro-3-hexenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | (E)-4-ethyl-2-hydroxyimino-5-nitro-3-hexenamide | HCID 86742405 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (E)-4-ethyl-2-methoxyimino-5-nitro-3-hexenamide | HCID 86742404 | — |
Reaction Steps
To (E)-4-ethyl-2-hydroxyimino-5-nitro-3-hexenamide (37 mg) in methanol (5 ml) was added excess etheral diazomethane at -20° C. The resulting mixture was allowed to stand at 0° C. for an hour and then acetic acid was added thereto until the yellow color of the solution was discharged. The resulting reaction mixture was evaporated under reduced pressure to give an oil which was purified by preparative thin layer chromatography, developing with chloroform containing 5% methanol to give (E)-4-ethyl-2-methoxyimino-5-nitro-3-hexenamide (21.5 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04767768 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-f25cf4e8ebf54c4fb1344e4967d7d306 |
| Source note | uspto-grants-1988_08 |