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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ethylhydroxylamine hydrochlorideHCID 76850—
ReactantSodium AcetateHCID 517045—
ReactantHCID 178458846HCID 178458846—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product2-[1-(Ethoxyimino)propyl]-3-hydroxy-5-[3-methanesulfonamido-2,4,6-trimethylphenyl]cyclohex-2-en-1-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888043
Source datasetuspto-grants-1989_12
ORD IDord-01025e891b464796bd275ba0a3c05ea3
Source noteuspto-grants-1989_12