3,4-Dichloroaniline → 2-[N-(3,4-dichlorophenyl)amino]pentanoic Acid Iso-butyl Ester
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[Cl:9])[NH2:5].O=[C:11]([CH2:19][CH2:20][CH3:21])[C:12]([O:14][CH2:15][CH:16]([CH3:18])[CH3:17])=[O:13]>>[CH2:15]([O:14][C:12](=[O:13])[CH:11]([NH:5][C:4]1[CH:6]=[CH:7][C:8]([Cl:9])=[C:2]([Cl:1])[CH:3]=1)[CH2:19][CH2:20][CH3:21])[CH:16]([CH3:18])[CH3:17]Komponenten
3
Versuchsvorschrift
Following General Procedure AA above and using 3,4-dichloroaniline (Aldrich) and iso-butyl 2-oxopentanoate (prepared by following General Procedure AO above using 2-oxovaleric acid (Fluka) and iso-butanol), the title compound was prepared as an oil. The reaction was monitored by tlc on silica gel (Rf=0.5 in 25% EtOAc/hexanes) and purification was by preparative plate chromatography (silica gel using 25% EtOAc/hexanes as the eluant).
Aufarbeitung
- customThe reaction was monitored by tlc on silica gel (Rf=0.5 in 25% EtOAc/hexanes) and purification
Quellen und Nachweise
- ORD-Eintrag
- ord-4731f2d86d7f4be485a88ac4477ff761
- Quelldatensatz
- uspto-grants-2003_11
- Patentnummer
- US06653303B1
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