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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111035Generated: October 31, 2026

Pyridine → HCID 86744414, compound

https://huagongshe.com/reaction/1111035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 22154861HCID 22154861—
ReactantHCID 86744413HCID 86744413—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86744414HCID 86744414—

Reaction Steps

A solution of 0.1 mol of p-aminobenzaldehyde ethylene glyco acetal in 100 mL of anhydrous THF is added dropwise over 10 minutes to a solution of 0.1 mol of isoleucine allyl 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'-[1-(allyloxycarbonyl)-1-methylbutyl]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-31e195b929784f2091ade2dd8d619960
Source noteuspto-grants-1990_12