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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993903Generated: October 30, 2026

Ethylenediamine → (3-Chloro-phenyl)-(4,5-dihydro-1H-imidazol-2-ylmethyl)-methyl-amine

https://huagongshe.com/reaction/1993903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantTrimethylaluminumHCID 16682925—
Reactant[(3-Chloro-phenyl)-methyl-amino]-acetic acid ethyl esterHCID 68536230—
SolventTolueneHCID 1140—
Product(3-Chloro-phenyl)-(4,5-dihydro-1H-imidazol-2-ylmethyl)-methyl-amineHCID 2516844629.4%

Reaction Steps

To dry toluene (4 ml) under an inert atmosphere at 0° C. was added a toluene solution of trimethylaluminium (2.13 ml, 4.26 mmol, 2 M solution). A solution of ethylenediamine (0.29 ml, 4.26 mmol) in toluene (1.5 ml) was then added dropwise and the reaction mixture was then allowed to warm to room temperature and stirred for 100 min at this temperature before being re-cooled to 0° C. To this mixture was added dropwise a solution of [(3-chloro-phenyl)-methyl-amino]-acetic acid ethyl ester (0.49 g, 2.13 mmol) in toluene (3 ml). The reaction mixture was then heated at reflux for 2.5 h and then cooled first to room temperature and finally to 0° C. The mixture was quenched by dropwise addition of methanol (1 ml) and when all gas evolution had ceased the mixture was diluted with water and extracted twice with ethyl acetate. The combined organic extracts were dried over sodium sulphate, filtered and concentrated in vacuo. The residue was triturated in ether to yield a white solid (0.14 g, 29%) which was collected by filtration; MS (ISP): 226.2, 224.1 ([M+H]+.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652055B2
Source datasetuspto-grants-2010_01
ORD IDord-2de6d6d56e1c4183b7a183b99b8d7720
Source noteuspto-grants-2010_01