Sodium Hydroxide → 4-[(5-Nitro-1H-indol-1-yl)methyl]benzoic acid
Reaction equation
[OH-].[Na+].[N+:3]([C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[N:11]([CH2:15][C:16]1[CH:25]=[CH:24][C:19]([C:20]([O:22]C)=[O:21])=[CH:18][CH:17]=1)[CH:10]=[CH:9]2)([O-:5])=[O:4]>>[N+:3]([C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[N:11]([CH2:15][C:16]1[CH:25]=[CH:24][C:19]([C:20]([OH:22])=[O:21])=[CH:18][CH:17]=1)[CH:10]=[CH:9]2)([O-:5])=[O:4]Participants
3
Procedure
4-[(5-Nitro-1H-indol-1-yl)methyl]benzoic acid was prepared by NaOH hydrolysis of methyl 4-[(5-nitro-1H-indol-1-yl)methyl]benzoate: MS (ESI) m/z 295;
Sources & evidence
- ORD record
- ord-447ced336f944199b0911342feb7962f
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07683091B2
Reaction notes
Loading…