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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649679Generated: October 29, 2026

p-Aminoacetophenone → N-[4-(1-hydroxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylurea

https://huagongshe.com/reaction/649679

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-AminoacetophenoneHCID 7468—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantGlycine isopropyl ester isocyanateHCID 86742133—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-(1-hydroxyiminoethyl)phenyl]-N'-isopropoxycarbonylmethylureaHCID 72742602—

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 glycine isopropyl 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'-isopropoxycarbonylmethylurea, which is isolated by filtration and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04740611
Source datasetuspto-grants-1988_04
ORD IDord-ea2602fd17ad416084025b5176c0aee3
Source noteuspto-grants-1988_04