4-Chloropyridine → 4-(Diallylamino)pyridine

HRID 280900Notes

Reaction equation

HRID 280900 reaction equation
Cl[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.[CH2:8]([NH:11][CH2:12][CH:13]=[CH2:14])[CH:9]=[CH2:10].[OH-].[Na+]>>[CH2:8]([N:11]([CH2:12][CH:13]=[CH2:14])[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1)[CH:9]=[CH2:10]

Participants

4

Procedure

4-Chloropyridine (13.24 g) was refluxed with excess diallylamine (28.04 g) under a nitrogen atmosphere for 3 days. The product mixture was neutralized with aqueous NaOH and extracted with ether. After drying, the ether was removed by simple distillation and the product purified by fractional distillation under reduced pressure. The pure 4-(diallylamino)pyridine (DAAP) was characterized by elemental analysis, FTIR, 13C NMR, and GC.

Workup

  1. extractionextracted with ether
  2. customAfter drying
  3. customthe ether was removed by simple distillation
  4. distillationthe product purified by fractional distillation under reduced pressure

Sources & evidence

ORD record
ord-6f582606bbbb4b84a7745dc734b69fdf
Source dataset
uspto-grants-1986_05
Patent number
US04591625

Reaction notes

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