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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-(4-Nitrophenyl)butanal | HCID 22269730 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3-(4-Nitrophenyl)propyl)-4,5-dihydro-1H-imidazole | HCID 57672606 | 76.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680291B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-7ff50ba2a7694d5b9ce7e550c9d08300 |
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| Source note | uspto-grants-2014_03 |
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