Water → HCID 86740955, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=O)[CH2:9][C:10]2[CH:15]=[N:14][CH:13]=[CH:12][N:11]=2)=[CH:4][CH:3]=1.Cl.[NH2:18][OH:19].C(=O)([O-])[O-].[Na+].[Na+].O>C(O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[N:18][OH:19])[CH2:9][C:10]2[CH:15]=[N:14][CH:13]=[CH:12][N:11]=2)=[CH:4][CH:3]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
10 g of 4'-chloro-2-(2-pyrazinyl)-acetophenone, 10 g of hydroxylamine hydrochloride and 12 g of anhydrous sodium carbonate are stirred at 60° in 100 ml of ethanol for 2 hours. The mixture is then treated with water and extracted with ethyl acetate, and the organic phase is dried over sodium sulfate and subsequently concentrated. The residue is crystallized from acetone/n-hexane to yield 4'-chloro-2-(2-pyrazinyl)-acetophenone oxime, m.p. 134°.
Aufarbeitung
- extractionextracted with ethyl acetate
- dry with materialthe organic phase is dried over sodium sulfate
- concentrationsubsequently concentrated
- customThe residue is crystallized from acetone/n-hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-88ab50000d52441ebfc6eb4441d5dce2
- Quelldatensatz
- uspto-grants-1986_08
- Patentnummer
- US04605656
Notizen zur Reaktion
Wird geladen…