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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108384Generated: October 30, 2026

Methanol → 1-(2-Methyl-pyridin-4-yl)-ethanone oxime

https://huagongshe.com/reaction/2108384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant1-(2-Methylpyridin-4-yl)ethan-1-oneHCID 20705014—
ReactantSodium Acetate TrihydrateHCID 23665404—
SolventWaterHCID 962—
SolventSodium chloride; waterHCID 57417360—
Product1-(2-Methyl-pyridin-4-yl)-ethanone oximeHCID 13635920067%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred suspension of 4-acetyl-2-methyl-pyridine [CAS No. 2732-28-7] (9.7 g, 71.8 mmol) in water (115 ml) was added at room temperature hydroxylamine hydrochloride (8.48 g, 122 mmol) and the mixture was heated to 70° C. At this temperature methanol (145 ml) was added dropwise over a period of 15 min and afterwards a solution of sodium acetate trihydrate (25.4 g, 187 mmol) in water (115 ml) was added dropwise over a period of 15 min. The reaction mixture was stirred at 80° C. for 3.5 h, brine (150 ml) was added and the solution was extracted with ethyl acetate (2×250 ml). The combined organic layers were washed with brine (150 ml), dried (MgSO4) and evaporated. The crude product was purified by crystallization from ethyl acetate/hexane to give 1-(2-methyl-pyridin-4-yl)-ethanone oxime (7.25 g, 67%) as an off-white solid; mp 154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514443B2
Source datasetuspto-grants-2009_04
ORD IDord-b77cabe33af04792a1dd03c65ea168da
Source noteuspto-grants-2009_04