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

HRID 2119213Notes

Reaction equation

HRID 2119213 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 pressre, 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 pressre
  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-30281a12fc9c4772a0183a24592562c4
Source dataset
uspto-grants-1987_07
Patent number
US04683310

Reaction notes

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