HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → HCID 4271757, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-hydroxy-N'-methyl-N-phenylurea | HCID 22632 | — |
| Product | HCID 4271757 | HCID 4271757 | — |
Reaction Steps
1-Methyl-3-phenyl-3-hydroxyurea (10 g; 0.06 mole) was dissolved in a cooled (10° C.) 2 N aqueous sodium hydroxide (0.068 mole) solution (34 ml.). Ethyl chloroformate (6.3 ml; 0.066 mole) was added dropwise at 10°-15° C. with stirring. The stirring was continued for about 1/2 hour after the addition was completed. The desired compound, which precipitated as formed, was removed by filtration, washed with water and dried. The compound was recrystallized from methanol and dried under vacuum to yield solid 2-phenyl-4-methyl-1,2,4-oxadiazolidine-3,5-dione having a melting point of 98°-99° C. and the following elemental analysis as calculated for C9H8N2O3 :
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04190431 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-89b8ce107ef045aa8f8ceca57cd0159a |
| Source note | uspto-grants-1980_02 |