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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409546Generated: October 27, 2026

Methyl 2-pyridylacetate → methyl 2-(N-hydroxyimino)-2-(pyridin-2-yl)acetate

https://huagongshe.com/reaction/1409546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-pyridylacetateHCID 74264—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
Productmethyl 2-(N-hydroxyimino)-2-(pyridin-2-yl)acetateHCID 13577878383%

Reaction Steps

To a solution of methyl 2-pyridylacetate (3.78 g) in acetic acid (15 mL) was added dropwise an aqueous solution (5 mL) of sodium nitrite (1.75 g) under ice-cooling, and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was neutralized with an aqueous sodium hydrogencarbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo, and the resultant crude product was purified by column chromatography on silica gel (solvent: hexane/ethyl acetate=75/25 to 25/75) to give methyl(hydroxyimino)(2-pyridyl)acetate (3.72 g, yield: 83%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921380B2
Source datasetuspto-grants-2014_12
ORD IDord-68cbbc9a54f0449992c8b093a26ec351
Source noteuspto-grants-2014_12