3-Nitrophenylacetic acid → 2-[(3Nitrophenyl)acetamido]butyric acid iso-butyl ester
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH2:10][C:11]([OH:13])=O)[CH:7]=[CH:8][CH:9]=1)([O-:3])=[O:2].[NH2:14][CH:15]([CH2:23][CH3:24])[C:16]([O:18][CH2:19][CH:20]([CH3:22])[CH3:21])=[O:17]>>[CH2:19]([O:18][C:16](=[O:17])[CH:15]([NH:14][C:11](=[O:13])[CH2:10][C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[CH:5]=1)[CH2:23][CH3:24])[CH:20]([CH3:21])[CH3:22]Participants
3
Procedure
Following General Procedure I above and using 3-nitrophenylacetic acid (Aldrich) and iso-butyl 2-aminobutyrate (prepared following General Procedure J above), the title compound was prepared. She reaction was monitored by tlc on silica gel and purification was by filtration as described in the general procedure. NMR data was as follows:
Workup
- customShe reaction
- customwas monitored by tlc on silica gel and purification
- filtrationwas by filtration
Sources & evidence
- ORD record
- ord-d440e91fcd8d4cec862249329831fa75
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06642261B2
Reaction notes
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