Hydroxyamine hydrochloride → 4-Phenoxyphenoxyacetaldehyde oxime
Reaktionsgleichung
Cl.[NH2:2][OH:3].C([O-])(=O)C.[Na+].[O:9]([C:16]1[CH:25]=[CH:24][C:19]([O:20][CH2:21][CH:22]=O)=[CH:18][CH:17]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>O.C(O)C>[O:9]([C:16]1[CH:25]=[CH:24][C:19]([O:20][CH2:21][CH:22]=[N:2][OH:3])=[CH:18][CH:17]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1Komponenten
6
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
A solution of 25 g of hydroxylamine hydrochloride and 29.4 g of anhydrous sodium acetate in 100 ml of water is added dropwise at room temperature to a solution of 68.5 g of 4-phenoxyphenoxyacetaldehyde in 300 ml ethanol. After the slightly exothermic reaction has subsided, the mixture is stirred for 2 hours at reflux temperature. The mixture is then cooled to 0° C. and stirred for 3 hours at this temperature, whereupon the resultant oxime crystallises. The crystallised 4-phenoxyphenoxyacetaldehyde oxime is isolated by suction filtration, repeatedly washed thoroughly with water and dried in a vacuum cabinet at 40° C. Melting point: 102°-105° C.
Aufarbeitung
- customAfter the slightly exothermic reaction
- temperatureat reflux temperature
- customcrystallises
Quellen und Nachweise
- ORD-Eintrag
- ord-e741c162d9384599acf5cbe2dcf8b8ec
- Quelldatensatz
- uspto-grants-1988_08
- Patentnummer
- US04766152
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