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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211047Generated: October 29, 2026

Ethylenediamine → N-(5-pyrimidinylmethyl)ethylenediamine

https://huagongshe.com/reaction/2211047

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. nD25 =5532.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05461167
Source datasetuspto-grants-1995_10
ORD IDord-1c0d8a7eca284abd8500f7184dd50011
Source noteuspto-grants-1995_10