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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947605Generated: November 3, 2026

Triethylamine → HCID 47125109, compound

https://huagongshe.com/reaction/1947605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-NitrophenoxyacetonitrileHCID 141854—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventMethanolHCID 887—
ProductHCID 47125109HCID 47125109—

Reaction Steps

O-Cyanomethyl-4-nitrophenol (8 g) was dissolved in methanol (50 mL) and to the solution was added hydroxyamine HCl (3.4 g) and triethylamine (9.4 mL). The reaction mixture was refluxed for 4 d and the solvent was removed under reduced pressure. The residue was redissolved in THF (50 mL). To the solution was added AcCl (23 mL) and triethylamine (50 mL). The reaction mixture was stirred at rt overnight, then added water (30 mL) and NaOH (18 g). The reaction solution was refluxed overnight, then diluted with water (200 mL). The aq. solution was extracted with EtOAc (2×150 mL). After separation, the combined EtOAc layers were dried, evaporated. The residue was purified by flash column chromatography (EtOAc/hexanes=1/2, 1/1, EtOAc) and recrystallized from EtOAc and hexanes to give O-(5-methyl-1,2,4-oxadiazol-3-yl)methyl-4-nitrophenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399472B2
Source datasetuspto-grants-2013_03
ORD IDord-369d24c7afac49fc97ffbec481199b4d
Source noteuspto-grants-2013_03