HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585698Generated: October 29, 2026
O-Methylhydroxylamine → HCID 86586324, compound
https://huagongshe.com/reaction/585698
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Methylhydroxylamine | HCID 4113 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | (+/-)-3-(2,4-Dihydroxyphenyl)cyclohexanone | HCID 12788196 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86586324 | HCID 86586324 | — |
Reaction Steps
(±)-3-(2,4-Dihydroxyphenyl)cyclohexanone (22 mg), methoxylamine hydrochloride (18 mg) and sodium acetate (18 mg) were heated under reflux in ethanol. After 6 hr, further methoxylamine (36 mg) and sodium acetate (36 mg) were added and the mixture heated under reflux for a further 1 hr. The reaction mixture was evaporated in vacuo and the residue was partitioned between ethyl acetate (20 ml) and water (20 ml). The aqueous layer was extracted with ethyl acetate (2×20 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 mixture of isomers (18 mg, 72%). δH (CDCl3) 1.5-2.2 (6H, overlapping m), 2.42 (0.5H, bd), 2.69 (0.5H, bd), 2.92 (0.5H, m), 3.06 (0.5H, m), 3.24-3.38 (1H, m), 3.81 (1.5H, s), 3.88 (1.5H, s), 5.42 (0.5H, bs), 5.47 (0.5H, bs), 6.28-6.42 (2H, overlapping m), 6.86 (0.5H, bs), 6.98 (1H, m), 7.06 (0.5H, bs); m/z (ES−) 469 (2M−1)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933319B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-4c97e8eeef22465189c7160757fa10f5 |
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| Source note | uspto-grants-2005_08 |
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