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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Chloride | HCID 312 | — |
| Reactant | 2-(6-Aminopyridin-2-yl)-2-methoxyiminoacetic acid hydrochloride | HCID 86737725 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(6-Amino-3-chloropyridin-2-yl)-2-methoxyiminoacetic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04395411 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-334526b3ccb14b3180c94184b2df965f |
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| Source note | uspto-grants-1983_07 |
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