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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433222Generated: October 29, 2026

4-[(2,5-Dioxoimidazolidin-1-yl)methyl]benzonitrile → 3-(4-Formylbenzyl)hydantoin

https://huagongshe.com/reaction/433222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(2,5-Dioxoimidazolidin-1-yl)methyl]benzonitrileHCID 2478718—
ReactantHCID 178527019HCID 178527019—
CatalystNickelHCID 935—
SolventHCID 67720230HCID 67720230—
Product3-(4-Formylbenzyl)hydantoinHCID 18758564—

Reaction Conditions

Temperature0 °C

Reaction Steps

The 3-(4-cyanobenzyl)hydantoin derivative obtained in step F (about 14 mmol) was dissolved in 360 ml of a mixture of pyridine/acetic acid/water (2/1/1), cooled to 0° C. and treated with 25.1 g of sodium hypophosphite (monohydrate) and 4.17 g of moist Raney nickel. After stirring at 60° C. for 6 h, the solvents were removed in vacuo and the residue was taken up in ethyl acetate. The solvent was washed with 10% strength citric acid solution, saturated sodium bicarbonate solution and saturated sodium chloride solution and dried over magnesium sulfate. After filtration and concentration, the 3-(4-formylbenzyl)hydantoin derivative obtained was employed in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667334B1
Source datasetuspto-grants-2003_12
ORD IDord-5e927dba59bc42b0832fb1ce884b1a2d
Source noteuspto-grants-2003_12