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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568835Generated: October 30, 2026

Sodium Hydroxide → 2-(2-Formamido-5-chlorothiazol-4-yl)-2-methoxyiminoacetic acid

https://huagongshe.com/reaction/568835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(2-formamido-5-chlorothiazol-4-yl)-2-methoxyiminoacetateHCID 54156297—
Product2-(2-Formamido-5-chlorothiazol-4-yl)-2-methoxyiminoacetic acidHCID 5387477586.1%

Reaction Steps

1N-Aqueous sodium hydroxide (195 ml.) was added dropwise to an aqueous suspension (190 ml.) of ethyl 2-(2-formamido-5-chlorothiazol-4-yl)-2-methoxyiminoacetate (18.9 g.) under ice-cooling and stirred for 4 hrs. The reaction mixture was washed with ethyl acetate, and ethyl acetate was added to the aqueous solution, adjusted to pH 1.0 with 6N-hydrochloric acid and then saturated with sodium chloride. The ethyl acetate layer was separated and the remaining aqueous layer was washed with ethyl acetate. The ethyl acetate layer obtained above and the washings were combined, washed with saturated aqueous sodium chloride, dried over magnesium sulfate and then evaporated in vacuo. The residue was pulverized with diisopropyl ether and the precipitates were collected by filtration and dried to give 2-(2-formamido-5-chlorothiazol-4-yl)-2-methoxyiminoacetic acid (syn isomer, 14.7 g.), m.p. 175° to 177° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04729991
Source datasetuspto-grants-1988_03
ORD IDord-33094a091b644c6fab92bef909c6e7c0
Source noteuspto-grants-1988_03