HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Ethyl-2-hydroxy-5-nitrohexanamide → HCID 14329816, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Ethyl-2-hydroxy-5-nitrohexanamide | HCID 19851670 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 14329816 | HCID 14329816 | 14% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a solution of 4-ethyl-2-hydroxy-5-nitrohexanamide (0.36 g) in acetic acid (5 ml) was added chromium trioxide (0.23 g). The resulting mixture was heated at 100° C. for 40 minutes with stirring. After cooling, the mixture was evaporated to dryness. The resulting residue was diluted with water and then extracted with ethyl acetate. The extract was washed successively with water, an aqueous sodium bicarbonate and brine, and then dried over magnesium sulfate. The solvent was removed by distillation to give an oil. The oil was purified by a preparative thin layer chromatography [solvent: methanol-chloroform (5:95)] to give 4-ethyl-5-nitro-2-oxo-hexanamide (50 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04767768 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-df76dae2b71d4ef2ab054c4e19605431 |
| Source note | uspto-grants-1988_08 |