Potassium Hydroxide → HCID 15480127, compound
Reaction equation
[CH2:1]([N:8]([CH2:10][C:11]1[C:16]([CH3:17])=[C:15](Br)[CH:14]=[C:13]([N+:19]([O-])=O)[C:12]=1[NH2:22])[CH3:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[K+]>[Ni]>[CH2:1]([N:8]([CH2:10][C:11]1[C:16]([CH3:17])=[CH:15][CH:14]=[C:13]([NH2:19])[C:12]=1[NH2:22])[CH3:9])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-[(Benzyl-methyl-amino)-methyl]-4-bromo-3-methyl-6-nitro-phenylamine (6 g, 16.5 nmnol) was hydrogenated (Ra Ni, 3 g) in the presence of KOH (0.498N). Reaction mixture filtered and extracted in CHCl3 (200 mL) and washed with water and dried (MgSO4). Solvent evaporated to give a dark oil 4.19 g=99%.
Workup
- customReaction mixture
- filtrationfiltered
- extractionextracted in CHCl3 (200 mL)
- washwashed with water
- dry with materialdried (MgSO4)
- customSolvent evaporated
Sources & evidence
- ORD record
- ord-4dad01329a5741c1abc7a96995ed41eb
- Source dataset
- uspto-grants-2001_01
- Patent number
- US06172065B2
Reaction notes
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