Reaktionsgleichung
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.Cl.[NH2:11][OH:12].N1C=CC=CC=1.Cl>C(Cl)Cl>[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=[N:11][OH:12])=[CH:4][CH:3]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
4-Chlorobenzaldehyde (45.6 g; 0.325 mol), hydroxylamine hydrochloride (27.9 g; 0.401 mol) and pyridine (64 mL; 0.791 mol) in methylene chloride (600 mL) were stirred overnight at room temperature. The reaction mixture was poured into aqueous hydrochloric acid (2N; 300 mL) and extracted. The organic layer was washed with additional aqueous hydrochloric acid (2×300 mL), water (300 mL), dried (MgSO4), filtered and evaporated to yield oxime 1a as a white solid.
Aufarbeitung
- extractionextracted
- washThe organic layer was washed with additional aqueous hydrochloric acid (2×300 mL), water (300 mL)
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-dec01e3068d14e62ad5b13417df02795
- Quelldatensatz
- uspto-grants-2011_03
- Patentnummer
- US07902227B2
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