Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Hydantoic acid | HCID 10020 | — |
| Edukt | N-[[(3,5-dichlorophenyl)amino]carbonyl]glycine | HCID 595293 | — |
| Lösungsmittel | Chlorobenzene | HCID 7964 | — |
| Produkt | 3-(3,5-Dichlorophenyl)-2,4-imidazolidinedione | HCID 168691 | 95,6% |
Reaktionsschritte
To a suspension of 3-(3,5-dichlorophenyl)-ureidoacetic acid (813 g.) in chlorobenzene (3,500 cc.) is added concentrated sulphuric acid (d = 1.83) (16 cc.), representing 0.095 mol per mol of ureidoacetic acid. The water formed in the reaction is removed by azeotropic distillation. After 45 minutes' distillation, a limpid solution is obtained. After cooling to about 15° C, the precipitate formed is filtered off and washed on the filter with ethanol (500 cc.) at 10° C. After drying, 3-(3,5-dichlorophenyl)-hydantoin (724 g.) melting at 199° C is obtained. Yield: 95.4%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04099008 |
|---|
| Quelldatensatz | uspto-grants-1978_07 |
|---|
| ORD ID | ord-be996351cfeb41cdad920d3b577d1ac0 |
|---|
| Quellennotiz | uspto-grants-1978_07 |
|---|