HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Quinazolinedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Isatoic Anhydride | HCID 8359 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Quinazolinedione | HCID 64048 | 76.8% |
Reaction Steps
978 g of isatoic acid anhydride were added in portions with stirring at 150° C. to a mixture of 720 g of urea and 1 liter of dimethylformamide and the mixture was then heated at 180° C. until evolution of ammonia ceased. The mixture was cooled and one liter of water was immediately added thereto followed by the addition of one liter of methanol. The warm mixture was stirred for one hour and was then filtered. The product was rinsed with warm water and with methanol and was then added with stirring to 2-3 volumes of warm dimethylformamide. The mixture was filtered and the product was rinsed with methanol to obtain 747 g of quinazoline-2,4-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04350695 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-2e4e4b665e384aa3a6b5acea03e9fdad |
| Source note | uspto-grants-1982_09 |