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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111031Generated: November 1, 2026

Pyridine → HCID 86744410, compound

https://huagongshe.com/reaction/1111031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTetrahydrofuranHCID 8028—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 86744409HCID 86744409—
SolventMethanolHCID 887—
ProductHCID 86744410HCID 86744410—

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 alanine allyl ester isocyanate and 0.35 moI 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'-[1-(allyloxycarbonyl)ethyl]urea, 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-e4a24f7162184dfb9a0af30802d641ac
Source noteuspto-grants-1990_12