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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261850Generated: October 25, 2026

Hydrochloric Acid → 2-(2-Aminothiazole-4-yl)-2-methoxyiminoacetic acid

https://huagongshe.com/reaction/261850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(2-aminothiazol-4-yl)-2-methoxyiminoacetateHCID 581091—
ReactantHCID 178472869HCID 178472869—
SolventEthanolHCID 702—
Product2-(2-Aminothiazole-4-yl)-2-methoxyiminoacetic acidHCID 125216—

Reaction Steps

Ethanol (10 ml.) was added to a suspension of ethyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate (syn isomer), which can be represented as ethyl 2-methoxyimino-2-(2-imino-2,3-dihydrothiazol-4yl)acetate (syn isomer), (2.2 g.) in a 1N aqueous solution of sodium hydroxide (12 ml.) and the mixture was stirred for 15 hours at ambient temperature. The reaction mixture was adjusted to pH 7.0 with 10% hydrochloric acid and ethanol was distilled off under reduced pressure. The residual aqueous solution was washed with ethyl acetate, adjusted to pH 2.8 with 10% hydrochloric acid and stirred under ice-cooling to precipitate crystals. The crystals were collected by filtration, washed with acetone and recrystallized from ethanol to give colorless needles of 2-methoxyimino-2-(2-aminothiazol-4-yl)acetic acid (syn isomer), which can be represented as 2-methoxyimino-2-(2-imino-2,3-dihydrothiazol-4-yl)acetic acid (syn isomer), (1.1 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152433
Source datasetuspto-grants-1979_05
ORD IDord-c7eb4212d99a48119440e33386823026
Source noteuspto-grants-1979_05