HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydantoin → 3-(4-Nitrobenzyl)imidazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydantoin | HCID 10006 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(4-Nitrobenzyl)imidazolidine-2,4-dione | HCID 10752207 | 57.9% |
Reaction Steps
A solution of hydantoin (5.0 g, Aldrich) in 2N aqu. NaOH (25 ml) was stirred at room temperature for 1 hour, then a solution of p-nitrobenzyl bromide (10.8 g, Aldrich) in methanol (50 ml) was added and the mixture refluxed for 16 hours. The mixture was cooled and the pale yellow precipitate filtered off, dried in vacuo, and recrystalised from ethanol to give the desired product as pale yellow crystals (6.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05225431 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-86d2fe63c1234c87a9d1b4441aa934dc |
| Source note | uspto-grants-1993_07 |