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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247222Generated: October 30, 2026

p-Aminoacetophenone → HCID 86742139, compound

https://huagongshe.com/reaction/247222

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-AminoacetophenoneHCID 7468—
ReactantTetrahydrofuranHCID 8028—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 131715387HCID 131715387—
SolventPyridineHCID 1049—
ProductHCID 86742139HCID 86742139—

Reaction Steps

A solution of 0.02 mol 4-aminoacetophenone in 40 mL THF is added dropwise to a solution of 0.02 mol of 0-acetyltyrosine methyl ester isocyanate and 5 mL pyridine in 40 mL THF, and the reaction mixture is stirred for 3 hours. The solvent is then removed by rotary evaporator. The residue is dipersed in 50 ml CH3OH, and ) 0.022 mol hydroxylamine hydrochloride and 0.06 mol trimethyl orthoformate are added. The reaction mixture is heated to reflux for 1 hour. The solvent is removed by rotary evaporator. Addition of water to the residue results in precipitation of N-[4-(1-hydroxyiminoethyl)phenyl]-N'-[1-methoxycarbonyl-2-(4-acetyloxyphenyl)ethyl]urea, which is then treated with NaOCH3 to adjust the pH to 10. The solution is heated to reflux for 2.5 hours, and the solvent is removed under vacuum. The residue is washed with cold water to yield the crude 3-[4-(1-hydroxyiminoethyl)phenyl]-5-(4-acetyloxyphenyl)methylhydantoin. The hydantoin is purified by recrystallization from CH3OH:H2O.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04705864
Source datasetuspto-grants-1987_11
ORD IDord-70024c65c82746908507506d34de0408
Source noteuspto-grants-1987_11