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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286655Generated: November 1, 2026

Sodium Hydroxide → 2-(6-Formamidopyridin-2-yl)-2-ethoxyiminoacetic acid

https://huagongshe.com/reaction/2286655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantO-ethylhydroxylamine hydrochlorideHCID 76850—
ReactantEthyl 2-(6-formamidopyridin-2-yl)glyoxylateHCID 13060174—
SolventEthanolHCID 702—
Product2-(6-Formamidopyridin-2-yl)-2-ethoxyiminoacetic acidHCID 5365953545.4%

Reaction Steps

1 N Sodium hydroxide solution (8.5 ml.) was added to a stirred solution of ethyl 2-(6-formamidopyridin-2-yl)-glyoxylate (1.9 g.) in ethanol (30 ml.) at room temperature and stirred at the same temperature for 30 minutes. After adding ethoxylamine hydrochloride (912 mg.) to the solution, the solution was stirred at room temperature for 4 hours. The resultant solution was concentrated under reduced pressure, and ethyl acetate and an aqueous solution of sodium bicarbonate were added to the residue. The aqueous layer was separated and ethyl acetate was added to the solution. The solution was adjusted to pH 1 with 10% hydrochloric acid. The ethyl acetate layer was separated, dried over magnesium sulfate and concentrated under reduced pressure. The residue was triturated with a mixture of diethyl ether and petroleum ether to give 2-(6-formamidopyridin-2-yl)-2-ethoxyiminoacetic acid (920 mg.), mp 155° to 156° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04267176
Source datasetuspto-grants-1981_05
ORD IDord-2c91bc77e7a74ae692ef997ba74ae1c2
Source noteuspto-grants-1981_05