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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 238930Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/238930

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroxyamine hydrochlorideHCID 443297—
EduktN-(4-acetylphenyl)methanesulfonamideHCID 684083—
LösungsmittelWaterHCID 962—
LösungsmittelPyridineHCID 1049—
ProduktN-{4-[1-(hydroxyamino)ethylidene]cyclohexa-2,5-dien-1-ylidene}methanesulfonamideHCID 6612326—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642657B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-8be3c1feb80d41cca7259ae6441eb595
Quellennotizuspto-grants-2014_02