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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantMethyl 4-(2-oxoimidazolidin-1-yl)benzoateHCID 18526090—
ReactantIodo-1-tert-butyl-4-iodobenzeneHCID 68689466—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 4-(3-(4-tert-butylphenyl)-2-oxoimidazolidin-1-yl)benzoateHCID 59456842—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790707B2
Source datasetuspto-grants-2010_09
ORD IDord-dabb1a89e9dd4857a393e4a8d7cfebce
Source noteuspto-grants-2010_09