HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661866Generated: October 25, 2026
2,6-Dibromotoluene → 1-Benzyl-3-(3-bromo-2-methylphenyl)imidazolidin-2-one
https://huagongshe.com/reaction/661866
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dibromotoluene | HCID 34681 | — |
| Reactant | 1,2-Diaminocyclohexane, trans- | HCID 43806 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-Benzylimidazolidin-2-one | HCID 231403 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-Benzyl-3-(3-bromo-2-methylphenyl)imidazolidin-2-one | HCID 59375087 | 25% |
Reaction Steps
Step 2 A mixture of 1,3-dibromo-2-methylbenzene (0.147 mL, 1.064 mmol), 1-benzylimidazolidin-2-one (75 mg, 0.426 mmol), copper (I) iodide (8.11 mg, 0.043 mmol), (+/−)-trans-1,2-diaminocyclohexane (5.1 mL, 0.043 mmol) and tripotassium phosphate (181 mg, 0.851 mmol) in dioxane (2 mL) was sonicated while bubbling with argon for 1 min. The mixture was heated in a sealed tube at 120° C. After 18.25 h, the mixture was cooled to rt, diluted with EtOAc and filtered through Celite. The filtrate was concentrated and the residue was purified by column chromatography (eluting with a gradient from 20:80 EtOAc-hexane to EtOAc) to provide 1-benzyl-3-(3-bromo-2-methylphenyl)imidazolidin-2-one as a waxy white solid (36 mg, 25%). 1H NMR (400 MHz, chloroform-d) δ 7.49 (1H, dd, J=7.9, 0.9 Hz), 7.28-7.40 (5H, m), 7.19 (1H, dd, J=7.8, 1.0 Hz), 7.08 (1H, t, J=7.9 Hz), 4.46 (2H, s), 3.64 (2H, dd, J=8.8, 6.8 Hz), 3.37 (2H, dd, J=8.8, 7.0 Hz), 2.36 (3H, s). Mass spectrum m/z 346.8 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084620B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-4bd46993af404a0198e6a360d8556fc2 |
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| Source note | uspto-grants-2011_12 |
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