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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427146Generated: November 2, 2026

4-[4-(4-Cyanophenyl)-2,5-dioxo-3-methyl-4-[(2-propenyloxy)methyl]imidazolidin-1-yl]-2-trifluoromethylbenzonitrile → 4-[4-(4-Cyanophenyl)-2,5-dioxo-4-hydroxymethyl-3-methylimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

https://huagongshe.com/reaction/2427146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[4-(4-Cyanophenyl)-2,5-dioxo-3-methyl-4-[(2-propenyloxy)methyl]imidazolidin-1-yl]-2-trifluoromethylbenzonitrileHCID 67130912—
SolventDichloromethaneHCID 6344—
Product4-[4-(4-Cyanophenyl)-2,5-dioxo-4-hydroxymethyl-3-methylimidazolidin-1-yl]-2-trifluoromethylbenzonitrileHCID 59317179—

Reaction Steps

To a solution of 433 mg of 4-[4-(4-cyanophenyl)-2,5-dioxo-3-methyl-4-[(2-propenyloxy)methyl]imidazolidin-1-yl]-2-trifluoromethylbenzonitrile obtained in Step 5 in DCM (5 mL), 600 μL of boron trifluoride-dimethyl sulfide complex is added. The mixture is stirred 8 hours at rt, diluted with DCM, washed with an aqueous solution of sodium bicarbonate, dried over magnesium sulfate, concentrated and purified on silica gel (ethyl acetate/cyclohexane: 0/100 to 50/50) to give the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968581B2
Source datasetuspto-grants-2011_06
ORD IDord-6cba6f7d0a2743819af07a5d818daf0f
Source noteuspto-grants-2011_06