HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227454Generated: November 1, 2026
Methane → 4-Ethyl-4-phenyl-2-(2-phenylquinolin-4-yl)-imidazoline
https://huagongshe.com/reaction/2227454
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methane | HCID 297 | — |
| Reactant | 2-Phenylbutane-1,2-diamine | HCID 21149 | — |
| Reactant | Methyl 2-phenyl-4-quinolinecarboxylate | HCID 609693 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Ethyl-4-phenyl-2-(2-phenylquinolin-4-yl)-imidazoline | HCID 178435244 | — |
Reaction Steps
2-Phenylbutane-1,2-diamine (328 mg, 2.0 mmol) in 4.4 mL of toluene is added dropwise to a stirred solution of trimethylaluminum (2.0 M, 1 mL) in 5 mL of toluene at below 10° C. under nitrogen. At the end of methane evolution, methyl-2-phenyl-4-quinolinecarboxylate (263 mg, 1 mmol) in 2 mL of toluene is gradually added at room temperature. The reaction mixture is refluxed for 3 hours under nitrogen. After cooling, the solution is treated with 1 mL of water, diluted with 1 mL of methanol and 1 mL of methylene chloride, and refluxed for 15 minutes. After separation of organic solvent and solvent evaporation, the residue is purified over silica gel chromatography eluting with 5-10% MeOH/CH2Cl2. The corresponding compound is obtained as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413982B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-3653a529e44440ccb38978cef2f77d49 |
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| Source note | uspto-grants-2002_07 |
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