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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111007Generated: October 28, 2026

Pyridine → N-[4-(hydroxyiminomethyl)phenyl]-N'-n-propoxycarbonylmethylurea

https://huagongshe.com/reaction/1111007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTetrahydrofuranHCID 8028—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 86742132HCID 86742132—
SolventMethanolHCID 887—
ProductN-[4-(hydroxyiminomethyl)phenyl]-N'-n-propoxycarbonylmethylureaHCID 86744397—

Reaction Steps

A solution of 0.1 mol of p-aminobenzaldehyde ethylene glycol acetal in 100 mL of anhydrous THF is added dropwise over 10 minutes to a solution of 0.1 mol of glycine n-propyl ester isocyanate and 0.35 mol pyridine in 100 mL THF at room temperature under N2. The reaction mixture is stirred at room temperature for 2 hours. After 2 hours the solvent is removed by rotary evaporator. A solution of 0.11 mmol hydroxylamine hydrochloride and 0.1 mol trimethyl orthoformate in CH3OH is added, and the reaction mixture is heated to reflux under N2 for 1 hour. The reaction mixture is reduced to about 1/4 volume by rotary evaporator, and water is added. The product, N-[4-(hydroxyiminomethyl)phenyl]-N'-n-propoxycarbonylmethylurea, is isolated by filtration and dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977272
Source datasetuspto-grants-1990_12
ORD IDord-8b000cacd3dc405b80f383c93bdc69f8
Source noteuspto-grants-1990_12