HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 136056433, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-Allylhydroxylamine hydrochloride | HCID 3084724 | — |
| Reactant | 2-Butyryl-3-hydroxy-4-(4-methoxyphenyl)cyclohex-2-ene-1-one | HCID 19854189 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136056433 | HCID 136056433 | 66.6% |
Reaction Steps
Triethylamine (1.2 g) was added to a solution of 2-butyryl-3-hydroxy-4-(4-methoxyphenyl)cyclohex-2-e-n-1-one (2.9 g) and O-allylhydroxylamine hydrochloride (1.2 g) in absolute ethanol (50 ml) at ambient temperature. After stirring overnight at this temperature, the ethanol was evaporated in vacuo, water was added to the residue and the aqueous solution was extracted with methylene chloride. The organic extracts were dried over anhydrous magnesium sulphate and then evaporated in vacuo. The residue was chromatographed on a silica gel column using 10% Et2O--CH2Cl2 as eluant to give the title compound (2.3 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04921524 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-8b953e3462cd479cb7bf9f1310307946 |
| Source note | uspto-grants-1990_05 |