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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891255Generated: November 1, 2026

Methyl iodide → 1-(4-Bromobenzyl)-3-methylimidazolidine-2,4-dione

https://huagongshe.com/reaction/1891255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(4-Bromobenzyl)imidazolidine-2,4-dioneHCID 15406722—
SolventDimethylformamideHCID 6228—
Product1-(4-Bromobenzyl)-3-methylimidazolidine-2,4-dioneHCID 6681322083.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

1-(4-Bromobenzyl)imidazolidine-2,4-dione (1B4) (1.86 mmol, 500 mg) was dissolved in DMF (7 ml) and potassium carbonate (5.57 mmol, 770 mg) and iodomethane (1B5) (1.86 mmol, 0.116 ml, 264 mg) were added and the reaction mixture was stirred at 50° C. under nitrogen. The reaction was monitored by TLC and after 48 h of heating some starting material remained. An additional 2 equivalents of iodomethane (3.72 mmol, 0.232 ml, 528 mg) was added and the mixture stirred at 75° C. under nitrogen overnight. The reaction mixture was cooled to room temperature, filtrated and concentrated, then purified on silica eluting with heptane/EtOAc/EtOH 5/4/1 to give 1-(4-bromobenzyl)-3-methylimidazolidine-2,4-dione (1B6) 438 mg, (83%); 1H NMR (400 MHz, CDCl3) 7.51 (d, 2H) 7.15 (d, 2H) 4.53 (s, 2H) 3.74 (s, 2H) 3.06 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507521B2
Source datasetuspto-grants-2013_08
ORD IDord-846543b8db8549048b3c8374cbea17aa
Source noteuspto-grants-2013_08