HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (+/-)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanone oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | (+/-)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanone | HCID 22337753 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (+/-)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanone oxime | HCID 86586318 | 94% |
Reaction Steps
Hydroxylamine hydrochloride (71 mg), triethylamine (0.17 ml) and (±)-3-[2,4-bis(methoxymethoxy)phenyl]cyclohexanone (200 mg) were heated under reflux in ethanol (8 ml). After 0.75 hr, the reaction mixture was evaporated in vacuo and the residue was partitioned between ethyl acetate (100 ml) and water (100 ml). The aqueous layer was extracted with ethyl acetate (2×100 ml), and the combined organic extracts were dried over magnesium sulfate and evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO2, ethyl acetate/petrol, 1:1 v/v) to furnish the title compound as a pale yellow oil (197 mg, 94%); m/z (ES+) 310 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06933319B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-986709c871d74a1487b5a190271c1589 |
| Source note | uspto-grants-2005_08 |