Reaktionsgleichung
[CH3:1][NH:2][C:3](=[O:21])/[C:4](/[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[O:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[N:5]/[O:6][CH3:7].[Br:22]Br>C(Cl)(Cl)(Cl)Cl>[CH3:1][NH:2][C:3](=[O:21])/[C:4](/[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[O:14][C:15]1[CH:16]=[CH:17][C:18]([Br:22])=[CH:19][CH:20]=1)=[N:5]/[O:6][CH3:7]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of (E)-N-methyl-2-(2-phenoxyphenyl)-2-methoxyiminoacetamide (500 mg) in carbon tetrachloride (3 ml) was cooled to 0° C., and bromine in carbon tetrachloride (1.27 mmol) was dropwise added thereto. The resulant mixture was stirred at the same temperature for 1 hour, washed with a saturated aqueous sodium hydrogencarbonate solution and extracted with dichloroethane. The solvent was dried and evaporated, and the residue was subjected to HPLC with a mixture of hexane and ethyl acetate to give 200 mg of the objective compound.
Aufarbeitung
- washwashed with a saturated aqueous sodium hydrogencarbonate solution
- extractionextracted with dichloroethane
- customThe solvent was dried
- customevaporated
- additionthe residue was subjected to HPLC with a mixture of hexane and ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-2f9723b7f25242b182baad4162596539
- Quelldatensatz
- uspto-grants-1996_08
- Patentnummer
- US05548078
Verknüpfte Notizen
Wird geladen…