Oxalic Acid → HCID 21411023, compound
Reaction equation
[CH2:1]([N:4]([CH2:8][CH:9]([OH:24])[CH2:10][CH:11]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:5][CH2:6][CH3:7])[CH2:2][CH3:3].[C:25]([OH:30])(=[O:29])[C:26]([OH:28])=[O:27]>C(OCC)(=O)C>[C:25]([O-:30])(=[O:29])[C:26]([O-:28])=[O:27].[CH2:1]([NH+:4]([CH2:8][CH:9]([OH:24])[CH2:10][CH:11]([C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[CH2:5][CH2:6][CH3:7])[CH2:2][CH3:3].[CH2:1]([NH+:4]([CH2:8][CH:9]([OH:24])[CH2:10][CH:11]([C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[CH2:5][CH2:6][CH3:7])[CH2:2][CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The N,N-di-n-propyl-4,4-diphenyl-2-hydroxybutylamine from Example 1 above was dissolved in 50 ml. of ethyl acetate and oxalic acid was added to the solution. The precipitated product was collected by filtration and was recrystallized from ethyl alcohol. Colorless crystalline N,N-di-n-propyl-4,4-diphenyl-2-hydroxybutylaminium oxalate was collected by filtration and dried. M.P. 121°-122° C.
Workup
- filtrationThe precipitated product was collected by filtration
- customwas recrystallized from ethyl alcohol
- filtrationColorless crystalline N,N-di-n-propyl-4,4-diphenyl-2-hydroxybutylaminium oxalate was collected by filtration
- customdried
Sources & evidence
- ORD record
- ord-4319e4a4652e43dda6ba5cc2bca208e9
- Source dataset
- uspto-grants-1977_09
- Patent number
- US04049827
Reaction notes
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