HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Nitraquazone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Dimethylformamide diethylacetal | HCID 70913 | — |
| Reactant | 1-(m-nitrophenyl)quinazoline-2,4(1H, 3H)-dione | HCID 12812377 | — |
| Solvent | Water | HCID 962 | — |
| Product | Nitraquazone | HCID 68765 | — |
Reaction Steps
A mixture of 2.8 g of 1-(m-nitrophenyl)quinazoline-2,4(1H, 3H)-dione, 40 ml of dry tetrahydrofuran and 4.4 g of N,N-dimethylformamide diethyl acetal was refluxed for 6 hours. After the reaction was complete, the solvent was distilled off from the reaction mixture under reduced pressure. To the residue obtained was added water to precipitate a crude product, which was then recrystallized from methanol to produce 2.8 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-98d4c0711cd64ff2a02d07e1d64b5170 |
| Source note | uspto-grants-1977_04 |