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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649691Generated: October 26, 2026

p-Aminoacetophenone → N-[4-(1-hydroxyiminoethyl)phenyl]-N'-(1-methoxycarbonyl-2-carbamoylethyl)urea

https://huagongshe.com/reaction/649691

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-AminoacetophenoneHCID 7468—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantAsparagine methyl ester isocyanateHCID 86741878—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-(1-hydroxyiminoethyl)phenyl]-N'-(1-methoxycarbonyl-2-carbamoylethyl)ureaHCID 86741883—

Reaction Steps

A solution of 2.7 g 4-aminoacetophenone in 40 mL is THF added dropwise to a solution of 0.02 mol of asparagine 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 dispersed 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 10 hours. 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-carbamoylethyl)urea, which is isolated by filtration and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04740611
Source datasetuspto-grants-1988_04
ORD IDord-9dafeabf17cf4a7b821cdcf6e393a8d2
Source noteuspto-grants-1988_04