1,3-Propanediamine → N-(5-trifluoromethyl-2-pyridylmethyl)trimethylenediamine

HRID 359522

Reaktionsgleichung

Reaktionsgleichung von HRID 359522
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:4]=[CH:5][C:6]([CH:9]=O)=[N:7][CH:8]=1.[NH2:13][CH2:14][CH2:15][CH2:16][NH2:17]>C1C=CC=CC=1>[F:1][C:2]([F:12])([F:11])[C:3]1[CH:4]=[CH:5][C:6]([CH2:9][NH:13][CH2:14][CH2:15][CH2:16][NH2:17])=[N:7][CH:8]=1

Komponenten

4

Versuchsvorschrift

5-Trifluoromethylpicoline aldehyde (3.5 g) was added dropwise at room temperature to a solution of trimethylenediamine (7.4 g) in benzene (70 ml). After the addition, the mixture was gradually heated with stirring, and then while separating water as an azeotrope, refluxed for 2 hours. Benzene was distilled off under reduced pressure, and then the residue was dissolved in ethanol (100 ml). With stirring at 10° to 15° C., sodium borohydride (0.9 g) was added little by little. The mixture was then stirred at room temperature for 2 hours. Ethanol was distilled off at less than 30° C. Dichloromethane was added to the residue, and a portion of it soluble in dichloromethane was separated. Dichloromethane was distilled off under reduced pressure, and volatile materials were removed at 1 mmHg and less than 60° C. to give N-(5-trifluoromethyl-2-pyridylmethyl)trimethylenediamine (3.5 g) as a colorless oil.

Aufarbeitung

  1. additionAfter the addition
  2. temperaturethe mixture was gradually heated
  3. customwhile separating water as an azeotrope
  4. temperaturerefluxed for 2 hours
  5. distillationBenzene was distilled off under reduced pressure
  6. dissolutionthe residue was dissolved in ethanol (100 ml)
  7. stirringWith stirring at 10° to 15° C.
  8. additionsodium borohydride (0.9 g) was added little by little
  9. stirringThe mixture was then stirred at room temperature for 2 hours
  10. distillationEthanol was distilled off at less than 30° C
  11. additionDichloromethane was added to the residue
  12. customa portion of it soluble in dichloromethane was separated
  13. distillationDichloromethane was distilled off under reduced pressure, and volatile materials
  14. customwere removed at 1 mmHg and less than 60° C.

Quellen und Nachweise

ORD-Eintrag
ord-b4d80a1c4d214490b7393fd0fafda9dc
Quelldatensatz
uspto-grants-1991_03
Patentnummer
US05001138

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