HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Benzylidenehydantoin → 5-(Phenylmethyl)-2,4-imidazolidinedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Benzylidenehydantoin | HCID 97857 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 5-(Phenylmethyl)-2,4-imidazolidinedione | HCID 73565 | 80% |
Reaction Steps
190 g (1 mole) of 5-benzylidene-hydantoin are dissolved in 2 l of a N sodium hydroxide solution and 95 g of wet Raney-nickel are added. The hydrogen uptake is terminated after about 6-8 hours (the reaction mixture is shaken at atmospheric pressure). The catalyst is filtered off and washed with N sodium hydroxide. The filtrate is acidified to pH 3 with concentrated hydrochloric acid. The precipitated white crystals are filtered off, dried and washed with cold water. Thus 152 g of the desired compound are obtained, yield 80%. Mp.: 187°-189° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04647694 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-71ee4f757d954a4cad118254b35ef831 |
| Source note | uspto-grants-1987_03 |