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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192882Generated: October 26, 2026

Ethylenediamine → 2-(3-(4-Nitrophenyl)propyl)-4,5-dihydro-1H-imidazole

https://huagongshe.com/reaction/1192882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantN-bromobutanimideHCID 67184—
Reactant4-(4-Nitrophenyl)butanalHCID 22269730—
SolventDichloromethaneHCID 6344—
Product2-(3-(4-Nitrophenyl)propyl)-4,5-dihydro-1H-imidazoleHCID 5767260676.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

The mixture of 4-(4-Nitrophenyl)butanal (64) (0.28 g, 1.45 mmol) and ethylene diamine (0.1 mL, 1.59 mmol) in dry dichloromethane (10 mL) was stirred at 0° C. for 30 min under argon. NBS (0.26 g, 1.59 mmol) was added to the mixture and the resulting solution was stirred overnight at 21° C. Reaction was quenched by the addition of saturated NaHCO3 solution. The mixture was extracted with dichloromethane. The organic layer was dried over MgSO4, and evaporated in vacuo. The residue was purified by flash column chromatography (ethanol:ethyl acetate:triethylamine, 1:1:0.2) to give 2-(3-(4-Nitrophenyl)propyl)-4,5-dihydro-1H-imidazole (62) (0.26 g, 76%): 1H NMR δ 8.14 (d, 2H, J=8.7 Hz) 7.35 (d, 2H, J=8.7 Hz) 3.59 (s, 4H), 2.79 (t, 2H, J=7.7 Hz) 2.26 (t, 2H, J=7.4 Hz) 1.96-2.05 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680291B2
Source datasetuspto-grants-2014_03
ORD IDord-7ff50ba2a7694d5b9ce7e550c9d08300
Source noteuspto-grants-2014_03