HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Nitraquazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(m-nitroanilino)-N-ethylbenzamide | HCID 13305678 | — |
| Solvent | Water | HCID 962 | — |
| Product | Nitraquazone | HCID 68765 | — |
Reaction Steps
To a solution of 2.9 g of 2-(m-nitroanilino)-N-ethylbenzamide and 25 ml of tetrahydrofuran was added 1.0 g of 50 % sodium hydride, and stirring was performed for 30 minutes at room temperature. To this was added dropwise under cooling 5.4 g of ethyl chlorocarbonate, and the mixture was allowed to stand for one hour at room temperature and then refluxed for 10 hours. After the reaction was complete, the solvent was evaporated from the reaction mixture under reduced pressure, and to the residue obtained was added water to prepicpitate a crude product. This product was recrystallized from methanol to give 2.5 g of 1-(m-nitrophenyl)-3-ethylquinazoline-2,4(1H, 3H)-dione as colorless prisms, melting at 193°-194° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04016166 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-0cf5d302d5a14ad78d22f3d4b362dcfb |
| Source note | uspto-grants-1977_04 |