Oxalic Acid → HCID 18986853, compound
Reaction equation
[CH2:1]([N:4]([CH2:8][CH2:9][CH2:10][C:11]1[CH:16]=[C:15]([Cl:17])[CH:14]=[CH:13][C:12]=1[O:18][CH2:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH2:5][CH2:6][CH3:7])[CH2:2][CH3:3].[C:27]([OH:32])(=[O:31])[C:28]([OH:30])=[O:29]>C(O)C>[C:27]([OH:32])(=[O:31])[C:28]([OH:30])=[O:29].[CH2:1]([N:4]([CH2:8][CH2:9][CH2:10][C:11]1[CH:16]=[C:15]([Cl:17])[CH:14]=[CH:13][C:12]=1[O:18][CH2:19][CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH2:5][CH2:6][CH3:7])[CH2:2][CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 0.50 g of N,N-di-n-propyl-3-[5-chloro-2-(2-phenylethoxy)phenyl]propylamine in 10 ml of ethanol, was added a solution of 120 mg of oxalic acid in 5 ml of ethanol. After evaporation of the solvent, the obtained crystals were recrystallized from ethyl acetate to give 380 mg of N,N-di-n-propyl-3-[5-chloro-2-(2-phenylethoxy)phenyl]propylamine oxalate.
Workup
- customAfter evaporation of the solvent
- customthe obtained crystals were recrystallized from ethyl acetate
Sources & evidence
- ORD record
- ord-f95dabded2a44a1784b096c0440c0537
- Source dataset
- uspto-grants-1996_02
- Patent number
- US05495046
Reaction notes
Loading…