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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22225Generated: October 25, 2026

Ethylenediamine → N-(5-pyrimidinylmethyl)ethylenediamine

https://huagongshe.com/reaction/22225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantPyrimidine-5-carboxaldehydeHCID 2761034—
SolventBenzeneHCID 241—
ProductN-(5-pyrimidinylmethyl)ethylenediamineHCID 1391089284.8%

Reaction Steps

Ethylenediamine (60 g) was dissolved in benzene (200 ml), and 5-formylpyrimidine (21.6 g) was added at room temperature. Subsequently, the mixture was heated, and refluxed for 3 hours while removing water as an azeotrope. After the reaction, benzene and the excess of ethylenediamine were distilled off under reduced pressure. The residue was dissolved in ethanol (200 ml). Sodium borohydride (8.4 g) was added portionwise to this solution at room temperature, and subsequently the mixture was stirred at room temperature for 5 hours. Ethanol was distilled off under reduced pressure. Dichloromethane (100 ml) was added to the residue, and a dichloromethane-soluble portion was separated. Dichloromethane was distilled off from the dichloromethane layer under reduced pressure to give N-(5-pyrimidinylmethyl)ethylenediamine (25.8 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428032
Source datasetuspto-grants-1995_06
ORD IDord-27d3f817215040c68e8c00bc79b7b9f9
Source noteuspto-grants-1995_06