HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 136026289, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | O-ethylhydroxylamine hydrochloride | HCID 76850 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Reactant | HCID 178450329 | HCID 178450329 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136026289 | HCID 136026289 | — |
Reaction Steps
3-Hydroxy-5-(3-pyridyl)-2-butyrylcyclohex-2-en-1-one (1.0 g) was stirred with O-ethylhydroxylamine hydrochloride (1.1 equiv) and sodium acetate trihydrate (1.1 equiv) in ethanol (30 ml) at room temperature for 12 hr. The mixture was poured into a dilute acetic acid solution, which was subsequently extracted with ether. The dried (MgSO4) organic extract was evaporated to give 2-[1-(ethoxyimino)-butyl]-3-hydroxy-5-(3-pyridyl)cyclohex-2-en-1-one as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04631081 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-97e415cfe0074e15a854ebe97df1cdee |
| Source note | uspto-grants-1986_12 |