HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710333Generated: November 3, 2026
N,N'-Dimethylethylenediamine → Methyl 4-(3-(4-tert-butylphenyl)-2-oxoimidazolidin-1-yl)benzoate
https://huagongshe.com/reaction/1710333
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Methyl 4-(2-oxoimidazolidin-1-yl)benzoate | HCID 18526090 | — |
| Reactant | Iodo-1-tert-butyl-4-iodobenzene | HCID 68689466 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 4-(3-(4-tert-butylphenyl)-2-oxoimidazolidin-1-yl)benzoate | HCID 59456842 | — |
Reaction Steps
Methyl 4-(2-oxoimidazolidin-1-yl)benzoate (220 mg, 1.0 mmole) was mixed with iodo-1-tert-butyl-4-iodobenzene (260 mg, 1.0 mmol), CuI (38 mg, 0.2 mmol), K3PO4 (426 mg, 2 mmol), N,N′-dimethyl ethylenediamine (17 mg, 0.2 mmol) and 1,4-dioxane (5 ml). The mixture was heated at 110° C. with stirring for 12 hours, and the solvent was removed in vacuum. The residue was suspended in dichloromethane and purified on ISCO system (5% methanol in dichloromethane) to give a pure product as a white crystalline (275 mg, 78%): 1H NMR (400 MHz, CDCl3) δ 8.05 (dd, 2H), 7.70 (dd, 2H), 7.36 (dd, 2H), 7.20 (dd, 2H), 4.02 (s, 4H), 3.90 (s, 3H), 1.30 (s, 9H). MS (ESI) m/z: Calculated: 352.18; Observed: 353.10 (M++1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790707B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-dabb1a89e9dd4857a393e4a8d7cfebce |
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| Source note | uspto-grants-2010_09 |
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