Reaktionsgleichung
[CH2:1]([P:3]([C:7]1[CH:12]=[C:11]([O:13][C:14]2[C:19]([Cl:20])=[CH:18][C:17]([Cl:21])=[CH:16][N:15]=2)[CH:10]=[CH:9][C:8]=1[N+:22]([O-:24])=[O:23])(=[O:6])[O:4]C)[CH3:2].[OH-].[K+]>CO>[CH2:1]([P:3]([C:7]1[CH:12]=[C:11]([O:13][C:14]2[C:19]([Cl:20])=[CH:18][C:17]([Cl:21])=[CH:16][N:15]=2)[CH:10]=[CH:9][C:8]=1[N+:22]([O-:24])=[O:23])(=[O:4])[OH:6])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of methyl P-ethyl-2-nitro-5-(3,5-dichloro-2-pyridyloxy)phenylphosphinate (0.6 g.), methanol (10 ml.) and 5% aqueous potassium hydroxide (10 ml.) is heated to 90° for 15 min. The basic aqueous solution is acidified and extracted with ether. The combined ether extracts are washed and dried and the solvent is evaporated off to give P-ethyl-2-nitro-5-(3,5-dichloro-2-pyridyloxy)phenyl-phosphinic acid.
Aufarbeitung
- temperatureis heated to 90° for 15 min
- extractionextracted with ether
- washThe combined ether extracts are washed
- customdried
- customthe solvent is evaporated off
Quellen und Nachweise
- ORD-Eintrag
- ord-577a8a0a5b2d426fa3818a3651ce8144
- Quelldatensatz
- uspto-grants-1986_01
- Patentnummer
- US04563310
Verknüpfte Notizen
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