2,5-Pyridinedicarboxylic acid → N,N,N',N'-tetraisoamyl pyridine-2,5-dicarboxamide

HRID 1248567Notes

Reaction equation

HRID 1248567 reaction equation
[N:1]1[CH:6]=[C:5]([C:7]([OH:9])=O)[CH:4]=[CH:3][C:2]=1[C:10]([OH:12])=O.[CH2:13]([NH:18][CH2:19][CH2:20][CH:21]([CH3:23])[CH3:22])[CH2:14][CH:15]([CH3:17])[CH3:16]>>[CH2:19]([N:18]([CH2:13][CH2:14][CH:15]([CH3:16])[CH3:17])[C:10]([C:2]1[CH:3]=[CH:4][C:5]([C:7]([N:18]([CH2:19][CH2:20][CH:21]([CH3:23])[CH3:22])[CH2:13][CH2:14][CH:15]([CH3:16])[CH3:17])=[O:9])=[CH:6][N:1]=1)=[O:12])[CH2:20][CH:21]([CH3:23])[CH3:22]

Participants

3

Procedure

N,N,N',N'-tetraisoamyl pyridine-2,5-dicarboxamide was prepared using the method of Example 1 from pyridine-2,5-dicarboxylic acid and diisoamylamine. The crude product in toluene solution was washed several times with 0.5M aqueous sodium hydroxide and then with 0.5M aqueous hydrochloric acid and water. The solution was then treated with charcoal and filtered. The solvent was distilled under reduced pressure, but the product, a brown oil, was not itself distilled. It was made up as a 0.2M solution in AROMASOL H and tested for extraction of copper in the presence of chloride ion using the method of Examples 6 and 7 except that AROMASOL H was used as solvent. The results are given in Table 3. The results indicate that this is a very weak extractant suitable for recovering copper from aqueous solution of high chloride ion concentrations.

Workup

  1. washThe crude product in toluene solution was washed several times with 0.5M aqueous sodium hydroxide
  2. additionThe solution was then treated with charcoal
  3. filtrationfiltered
  4. distillationThe solvent was distilled under reduced pressure
  5. distillationdistilled
  6. extractiontested for extraction of copper in the presence of chloride ion using the method of Examples 6 and 7 except that AROMASOL H
  7. customfor recovering copper
  8. concentrationfrom aqueous solution of high chloride ion concentrations

Sources & evidence

ORD record
ord-0639933fd5bb457babee2b35ded8d475
Source dataset
uspto-grants-1985_06
Patent number
US04525330

Reaction notes

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