Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231185Erstellt: 26. Oktober 2026

Ethylenediamine → N-(1-methyl-4-pyrazolylmethyl)trimethylenediamine

https://huagongshe.com/reaction/231185

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylenediamineHCID 3301—
EduktAcetonitrileHCID 6342—
Edukt1-Methyl-1H-pyrazole-4-carbaldehydeHCID 573117—
ProduktN-(1-methyl-4-pyrazolylmethyl)trimethylenediamineHCID 14207161—

Reaktionsschritte

At room temperature 11 g of 1-methyl-4-pyrazole carbaldehyde was slowly added to 37 g of ethylenediamine in 150 ml of dry acetonitrile. Molecular sieves 4A (a product of Wako Pure Chemicals, Co.) were added as a dehydrating agent to the solution. The mixture was stirred at room temperature for 2 hours, and filtered. Acetonitrile was distilled off under reduced pressure from the filtrate. To the residue was added 100 ml of ethanol, and then 4 g of sodium borohydride was added little by little at room temperature. The mixture was then stirred at room temperature for 2 hours, and ethanol was distilled off under reduced pressure. Water was added to the residue, and the mixture was extracted with dichloromethane. The solvent was distilled off from the dichloromethane layer, and the residue was vacuum-distilled to give 10 g of N-(1-methyl-4-pyrazolylmethyl)trimethylenediamine as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04845106
Quelldatensatzuspto-grants-1989_07
ORD IDord-1c6056e56aa143f5a55368f82175737e
Quellennotizuspto-grants-1989_07