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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427135Generated: November 2, 2026

4-Bromo-2-(trifluoromethyl)benzonitrile → 4-[2,5-Dioxo-4-(4-fluorophenyl)-4-[(2-propenyloxy)methyl]imidazolidin-1-yl]-2-trifluoromethylbenzonitrile

https://huagongshe.com/reaction/2427135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-(trifluoromethyl)benzonitrileHCID 22337825—
Reactant4-(4-Fluorophenyl)-4-[(2-propenyloxy)methyl]imidazolidine-2,5-dioneHCID 67131210—
CatalystHCID 178419072HCID 178419072—
SolventAmmoniaHCID 222—
SolventDimethylacetamideHCID 31374—
Product4-[2,5-Dioxo-4-(4-fluorophenyl)-4-[(2-propenyloxy)methyl]imidazolidin-1-yl]-2-trifluoromethylbenzonitrileHCID 67131049—

Reaction Conditions

Temperature160 °C

Reaction Steps

0.33 g of copper (I) oxide and 0.95 g of 4-bromo-2-trifluoromethylbenzonitrile are added to a solution of 1 g 4-(4-fluorophenyl)-4-[(2-propenyloxy)methyl]imidazolidine-2,5-dione obtained in step 3 in 3 mL of DMAC. The mixture is heated at 160° C. for 3 hours. After cooling, the mixture is diluted with a 50% aqueous ammonia solution and extracted with ethyl acetate. The organic layer is dried over sodium sulfate, filtered and evaporated. The crude product is purified by chromatography over silica gel while eluting with 2/1 heptane/ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968581B2
Source datasetuspto-grants-2011_06
ORD IDord-fec0a556e0914b4a9d55a02aacb70ad4
Source noteuspto-grants-2011_06