HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477406Generated: October 29, 2026
O-ethylhydroxylamine hydrochloride → 2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-[3-methanesulfonamido-2,4,6-trimethylphenyl]cyclohex-2-en-1-one
https://huagongshe.com/reaction/477406
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-ethylhydroxylamine hydrochloride | HCID 76850 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 178458846 | HCID 178458846 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-[3-methanesulfonamido-2,4,6-trimethylphenyl]cyclohex-2-en-1-one | HCID 136058354 | — |
Reaction Steps
Sodium acetate (0.19 g, 2.29 mmol) and ethoxyamine hydrochloride (0.22 g, 2.29 mmol) were added to a solution of 2-propionyl-3-hydroxy-5-(3-methylsulphonamido-2,4,6-trimethylphenyl)cyclohex-2-en-1-one (0.58 g, 1.53 mmol) in ethanol (25 ml) and methylene chloride (25 ml). Stirring was continued at 20° for 18 hrs. The solvent was removed under reduced pressure and the residue partitioned between chloroform and water. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to yield2-[1-(ethoxyimino)propyl]-hydroxy-5-[3-(methylsulphonamido)-2,4,6-trimethylphenyl]cyclohex-2-en-1-one as a brown oil (0.27 g, 42%). The compound was characterized by proton magnetic resonance spectroscopy. The spectroscopic data are recorded in Table 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04888043 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-01025e891b464796bd275ba0a3c05ea3 |
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| Source note | uspto-grants-1989_12 |
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