HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-[(2,5-Dioxoimidazolidin-1-yl)methyl]benzonitrile → 3-(4-Formylbenzyl)hydantoin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-[(2,5-Dioxoimidazolidin-1-yl)methyl]benzonitrile | HCID 2478718 | — |
| Reactant | HCID 178527019 | HCID 178527019 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | HCID 67720230 | HCID 67720230 | — |
| Product | 3-(4-Formylbenzyl)hydantoin | HCID 18758564 | — |
Reaction Conditions
| Temperature | 0 °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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06667334B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-5e927dba59bc42b0832fb1ce884b1a2d |
| Source note | uspto-grants-2003_12 |