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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075273Generated: November 1, 2026

Acetic Acid → 2-(6-Amino-3-chloropyridin-2-yl)-2-methoxyiminoacetic acid

https://huagongshe.com/reaction/1075273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantChlorideHCID 312—
Reactant2-(6-Aminopyridin-2-yl)-2-methoxyiminoacetic acid hydrochlorideHCID 86737725—
SolventWaterHCID 962—
Product2-(6-Amino-3-chloropyridin-2-yl)-2-methoxyiminoacetic acidHCID 53795924—

Reaction Steps

To a mixture of 2-(6-aminopyridin-2-yl)-2-methoxyiminoacetic acid hydrochloride (syn isomer), acetic acid (350 ml.) and water (10 ml.) was introduced chloride gas for 1.5 hours. After the removal of the excess of the chlorine gas by bubbling air into the reaction mixture, the solvent was distilled off. The residue was pulverized in diethyl ether and collected by filtration. After the addition of water and ethyl acetate to the resultant powder (9.8 g.), the aqueous layer was separated and washed with ethyl acetate. The ethyl acetate layer and washings were combined together, and further extracted with water. The aqueous layers were combined together and adjusted to pH 4 with 1 N aqueous solution of sodium hydroxide, and then the solvent was distilled off under reduced pressure. The remaining water in the residue was azeotropically removed with benzene three times to yield brownish powder which was dried in a desiccator to give 2-(6-amino-3-chloropyridin-2-yl)-2-methoxyiminoacetic acid (syn isomer) (3.27 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04395411
Source datasetuspto-grants-1983_07
ORD IDord-334526b3ccb14b3180c94184b2df965f
Source noteuspto-grants-1983_07