HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(m-nitrophenyl)quinazoline-2,4(1H, 3H)-dione | HCID 12812377 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dione | HCID 13272344 | 90.7% |
Reaction Steps
To a solution of 2.8 g of 1-(m-nitrophenyl)quinazoline-2,4(1H, 3H)-dione and 30 ml of dimethylformamide was added 0.6 g of approximately 55 % sodium hydride and the solution was stirred for 30 minutes at room temperature. To this was further added 3.6 g of allyl bromide, and the mixture was reacted for 2 hours at room temperature. Then, the solvent was distilled off from the resulting mixture under reduced pressure to leave a residue, to which was added water to precipitate a crude product. This product was recrystallized from methanol to yield 2.9 g of 1(m-nitrophenyl)-3 -allylquinazoline- 2,4(1H, 3H)-dione as light brown needles, melting at 165°-166° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04016166 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-c0bfb59fdce74feeaef789a5fb0ed9a2 |
| Source note | uspto-grants-1977_04 |