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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471832Generated: October 27, 2026

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

https://huagongshe.com/reaction/471832

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 numberUS08633175B2
Source datasetuspto-grants-2014_01
ORD IDord-d5a1382a5ec845199b121b1a86a5fb36
Source noteuspto-grants-2014_01