HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 178492212, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | HCID 642154 | HCID 642154 | — |
| Catalyst | Ammonium Sulfate | HCID 6097028 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178492212 | HCID 178492212 | 59% |
Reaction Steps
A solution of 1.16 g (0.010 mole) of 6H-1,2,4-oxadiazin-3,5(2H,4H)-dione, 5 mg ammonium sulfate, 1.47 g (0.012 mole) of p-methoxyaniline and 20 ml hexamethyldisilazane in 40 ml of freshly distilled dry dioxane is refluxed for 17 hours. After cooling, the dioxane and hexamethyldisilazane are removed in vacuo and the syrupy residue is dried on a vacuum pump for 2 hours. The resulting semi-solid residue is triturated with 100 ml of petroleum ether and filtered to give a yield of 1.3 g (59 percent) of 5-((4-methoxyphenyl)amino)-6H-1,2,4-oxadiazin-3(2H)-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04459403 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-e4a9ec64bdfa495cb6bfa9a8bf30333b |
| Source note | uspto-grants-1984_07 |