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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238930Generated: October 26, 2026

Hydroxyamine hydrochloride → N-{4-[1-(hydroxyamino)ethylidene]cyclohexa-2,5-dien-1-ylidene}methanesulfonamide

https://huagongshe.com/reaction/238930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantN-(4-acetylphenyl)methanesulfonamideHCID 684083—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductN-{4-[1-(hydroxyamino)ethylidene]cyclohexa-2,5-dien-1-ylidene}methanesulfonamideHCID 6612326—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 4′-(Methylsulfonylamino)acetophenone (13-5, 5 mmol) and hydroxylamine hydrochloride (0.695 g, 10 mmol) in pyridine (5 mL) was heated at 70° C. for 3 h. The reaction mixture was cooled to room temperature, diluted with H2O, and extracted with EtOAc several times. The combined organic layers were washed with H2O and brine, dried over MgSO4, filtered, and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel using EtOAc:hexanes (1:1) as eluant to 4′-Methylsulfonylamino)acetophenone oxime (13-8, LJO-299).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642657B2
Source datasetuspto-grants-2014_02
ORD IDord-8be3c1feb80d41cca7259ae6441eb595
Source noteuspto-grants-2014_02