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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255109Generated: October 30, 2026

Ethylenediamine → N-(2-Aminoethyl)-4-chlorobenzamide hydrochloride

https://huagongshe.com/reaction/2255109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
SolventDiethyl EtherHCID 3283—
ProductN-(2-Aminoethyl)-4-chlorobenzamide hydrochlorideHCID 570225130.6%

Reaction Steps

A solution of 6.2 ml (0.05 mol) of 4-chlorobenzoyl chloride in 150 ml of ether is added dropwise at -10° over a period of 0.5 hour to a solution of 10 ml (0.15 mol) of ethylenediamine in 150 ml of ether. The mixture is left to warm to room temperature, filtered and the white residue is rinsed twice with ether. After concentrating the ether solution, the residue is acidified with dilute hydrochloric acid and extracted several times with ethyl acetate in order to remove the neutral constituents. The aqueous phase is made alkaline with sodium hydroxide solution and extracted several times with chloroform. After evaporating the chloroform, converting the residue into the hydrochloride and recrystallization from ethanol/ether, there are obtained 1.8 g of N-(2-aminoethyl)-4-chlorobenzamide hydrochloride which is identical with the product obtained in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05238962
Source datasetuspto-grants-1993_08
ORD IDord-87730b0b2e494be4901dc4d3092e09e7
Source noteuspto-grants-1993_08