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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193962Generated: November 2, 2026

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

https://huagongshe.com/reaction/1193962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-PropanediamineHCID 428—
Reactant5-(Trifluoromethyl)pyridine-2-carbaldehydeHCID 14422792—
SolventBenzeneHCID 241—
ProductN-(5-trifluoromethyl-2-pyridylmethyl)trimethylenediamineHCID 1420716275.1%

Reaction Steps

5-Trifluoromethylpicolinealdehyde (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 refluxed for 2 hours while removing water that azeotroped. Benzene was distilled off under reduced pressure. The residue was dissolved in ethanol (100 ml), and sodium borohydride (0.9 g) was added little by little while the solution was stirred at 10° to 15° C. The mixture was then stirred at room temperature for 2 hours, and ethanol was distilled off at less than 30° C. Dichloromethane was added to the residue, and a portion 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04812454
Source datasetuspto-grants-1989_03
ORD IDord-c188263d82cb457ea80ef9543b71f9b5
Source noteuspto-grants-1989_03