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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462199Generated: November 2, 2026

P-Anisidine → HCID 178492212, compound

https://huagongshe.com/reaction/1462199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
ReactantHexamethyldisilazaneHCID 13838—
ReactantHCID 642154HCID 642154—
CatalystAmmonium SulfateHCID 6097028—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178492212HCID 17849221259%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04459403
Source datasetuspto-grants-1984_07
ORD IDord-e4a9ec64bdfa495cb6bfa9a8bf30333b
Source noteuspto-grants-1984_07