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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641406Generated: October 27, 2026

Hydroxyamine hydrochloride → (NZ)-N-[1-(3,5-difluoro-2-pyridinyl)ethylidene]hydroxylamine

https://huagongshe.com/reaction/1641406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
Reactant2-Cyano-3,5-difluoropyridineHCID 2783253—
ReactantHCID 178418573HCID 178418573—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(NZ)-N-[1-(3,5-difluoro-2-pyridinyl)ethylidene]hydroxylamineHCID 136068547—

Reaction Steps

To a solution of 3,5-difluoropicolinonitrile (10.0 g, 71.4 mmol) in THF (200 ml) was added methylmagnesium bromide (61.2 ml, 85.7 mmol) in THF solution at 0° C. The reaction was stirred at room temperature for 1.5 hours. Saturated sodium bicarbonate solution (50 ml) was added, extracted with ether (100 ml), and dried over sodium sulfate. The solvent was removed. The residue (11.2 g, 71.28 mmol), hydroxylamine hydrochloride (9.907 g, 142.6 mmol) and sodium acetate (11.70 g, 142.6 mmol) in EtOH (100 ml) and water (50 ml) was heated at reflux for 3 hours. The solvent was removed and diluted with 50 ml of saturated sodium bicarbonate and extracted with EtOAc (2×200 ml). After dried over sodium sulfate, the solvent was removed and the title compound was used directly in next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114989B2
Source datasetuspto-grants-2012_02
ORD IDord-014e7bd0d54a4379ab4d2e7d3486dcf6
Source noteuspto-grants-2012_02