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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995065Generated: October 30, 2026

4-Acetylpyridine → N-[1-(Pyridin-4-yl)ethylidene]hydroxylamine

https://huagongshe.com/reaction/1995065

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AcetylpyridineHCID 14282—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductN-[1-(Pyridin-4-yl)ethylidene]hydroxylamineHCID 24799761.5%

Reaction Steps

To a solution of 7.64 g. (110 mmole) of hydroxylamine hydrochloride in 150 ml. of methyl alcohol were added 5.94 g. (110 mmole) of sodium methylate and the mixture was stirred at room temperature for 10 minutes. A solution of 12.11 g. (110 mmoles) of 4-acetylpyridine in 50 ml. of methyl alcohol was added dropwise over 3 minutes and the reaction mixture was stirred at room temperature for 3 hours and at the reflux temperature for 2.5 hours. After the mixture had cooled, the precipitate of sodium chloride was separated by filtration and the filtrate was concentrated by evaporation to one-half of the original volume. The concentrate was diluted with 50 ml. of water and the solution concentrated to a volume of about 100 ml. This concentrate was chilled in an ice bath for 30 minutes and the precipitate of the oxime was separated by filtration in the cold. There were obtained 8.38 g. (61.5% yield) of 4-acetylpyridine oxime.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04402955
Source datasetuspto-grants-1983_09
ORD IDord-74e4c1bfb8224690af2002e6a0b81858
Source noteuspto-grants-1983_09