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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359522Generated: October 26, 2026

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

https://huagongshe.com/reaction/359522

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-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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001138
Source datasetuspto-grants-1991_03
ORD IDord-b4d80a1c4d214490b7393fd0fafda9dc
Source noteuspto-grants-1991_03