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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70299Generated: October 26, 2026

3-Bromoaniline → 1-(3-Bromophenyl)-2,4-imidazolidinedione

https://huagongshe.com/reaction/70299

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromoanilineHCID 11562—
ReactantChloroacetyl isocyanateHCID 78209—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Solvent1,4-DioxaneHCID 31275—
Product1-(3-Bromophenyl)-2,4-imidazolidinedioneHCID 67160991—

Reaction Steps

A solution of 3-bromoaniline (1.0 mL, 9.18 mmol) and chloroacetyl isocyanate (0.780 mL, 9.18 mmol) in dioxane (100 mL) was stirred at room temperature for 2 hr. Dioxane (50 mL) and DBU (3.40 mL, 23.0 mmol) were added and the solution stirred at room temperature for 16 hr. The solution was concentrated in vacuo and the residue taken up in EtOAc and H2O. The mixture was then acidified with 1N HCl, then the aqueous phase extracted with EtOAc. The combined organics were then washed with H2O and brine and dried over Na2SO4. The solution was concentrated in vacuo and the residue recrystallized from EtOAc/hexanes to give 1-(3-bromophenyl)-2,4-imidazolidinedione as a tan solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 4.42 (s, 2H), 7.24-7.30 (m, 2H), 7.50-7.52 (m, 1H), 7.87 (s, 1H), 11.27 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822518B2
Source datasetuspto-grants-2014_09
ORD IDord-0099e797fa604f86a89d2920633199f2
Source noteuspto-grants-2014_09