3,4-Dichloroaniline → 2-[N-(3,4dichlorophenyl)amino]butanoic Acid Iso-butyl Ester
Reaction equation
[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][CH3:20])[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][CH3:20])[CH:16]([CH3:18])[CH3:17]Participants
3
Procedure
Following General Procedure AA above and using 3,4-dichloroaniline (Aldrich) and iso-butyl 2-oxobutanoate (prepared by following General Procedure AO above using 2-oxobutyric acid (Aldrich) and iso-butanol), the title compound was prepared as an oil. The reaction was monitored by tlc on silica gel (Rf=0.3 in 25% EtOAc/hexanes) and purification was by preparative plate chromatography (silica gel using 25% EtOAc/hexanes as the eluant).
Workup
- customThe reaction was monitored by tlc on silica gel (Rf=0.3 in 25% EtOAc/hexanes) and purification
Sources & evidence
- ORD record
- ord-91ecabfb6037471b9c328cd5af691ec9
- Source dataset
- uspto-grants-2003_12
- Patent number
- US06667305B1
Reaction notes
Loading…