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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379302Generated: October 25, 2026

Ethylenediamine → N-(5-pyrimidinylmethyl)ethylenediamine

https://huagongshe.com/reaction/379302

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=1.5532.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297374B1
Source datasetuspto-grants-2001_10
ORD IDord-971c2b7026634e6da822bfff4940f186
Source noteuspto-grants-2001_10