HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-ethylhydroxylamine hydrochloride → HCID 136109317, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-ethylhydroxylamine hydrochloride | HCID 76850 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Reactant | HCID 178450309 | HCID 178450309 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136109317 | HCID 136109317 | — |
Reaction Steps
A mixture of 2-butyryl-5-(1,4-dimethylnaphth-2-yl)-3-hydroxycyclohex-2-en-1-one (0.25 g), ethoxyamine hydrochloride (1.3 equiv) and sodium acetate trihydrate (1.3 equiv) were stirred in ethanol (30 ml) at room temperature for 4 hr. The mixture was then immediately extracted with ether. The dried (MgSO4) organic extract was evaporated to give 5-(1,4-dimethylnaphth-2-yl)-2-[1-(ethoxyimino)butyl]-3-hydroxycyclohex-2-en-1-one as a pale yellow oil. The product was characterized by proton nuclear magnetic resonance spectroscopy and the spectroscopic data is recorded in Table 4, Example 10.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04640708 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-e92168529cb8454cb26c838eb4ed9cf6 |
| Source note | uspto-grants-1987_02 |