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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10176Erstellt: 24. Oktober 2026

Water → acetophenone O-[2-((morpholin-4-yl))ethyl]oxime

https://huagongshe.com/de/reaction/10176

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium HydroxideHCID 14798—
EduktAcetophenonoximeHCID 69185—
EduktMorpholine, 4-(2-chloroethyl)-, hydrochloride (1:1)HCID 77210—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelTolueneHCID 1140—
Produktacetophenone O-[2-((morpholin-4-yl))ethyl]oximeHCID 86594237—

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

To a solution of acetophenone oxime (20 g) in toluene (700 mL) was added subsequently tetrabutylammonium bromide (4.77 g), water (8 mL), 4-(2-chloroethyl)morpholine hydrochloride (30.31 g) and finally 50% sodium hydroxide (aq, 52 mL). The resulting mixture was heated at 75° C. overnight. After cooling to room temperature water was added, to dissolve all the salts, the layers were separated, and the aqueous layer was extracted with toluene. The organic layers were dried (MgSO4), and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, CH2Cl2/MeOH 95/5) to afford acetophenone O-[2-((morpholin-4-yl))ethyl]oxime as an oil. The obtained oil was dissolved in 6M HCl (aq, 500 mL) and heated under reflux for 5 hours and subsequently stirred overnight at room temperature. The mixture was extracted with ether and concentrated in vacuo. The residue was crystallized from ethanol, to afford O-[2-((morpholin-4-yl))ethyl]hydroxylamine dihydrochloride. 24.8 g (77%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094779B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-7cdc52eb0f104415883f65036a3b8c9b
Quellennotizuspto-grants-2006_08