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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638431Generated: October 27, 2026

Hydrochloric Acid → 2-(2-Formylamino-5-chlorothiazol-4-yl)-2-oxoacetic Acid

https://huagongshe.com/reaction/638431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl (2-formamido-5-chlorothiazol-4-yl)glyoxylateHCID 14326717—
ReactantHCID 178473048HCID 178473048—
SolventPotassium HydroxideHCID 14797—
Product2-(2-Formylamino-5-chlorothiazol-4-yl)-2-oxoacetic AcidHCID 19790221—

Reaction Steps

Ethyl 2-(2-formylamino-5-chloro-1,3-thiazol-4-yl)-glyoxylate, which can be represented as ethyl 2-(2-formylimino-5-chloro-2,3-dihydro-1,3-thiazol-4-yl)glyoxylate, (1.3 g.) was dissolved in 1N potassium hydroxide aqueous solution (10 ml.) at room temperature with stirring and the solution was stirred for 5 minutes at the same temperature. After the reaction, the reaction mixture was cooled with ice and then adjusted to pH 1 with 10% hydrochloric acid. The precipitates were collected by filtration, washed with water and then dried to give 2-(2-formylamino-5-chloro-1,3-thiazol-4-yl)glyoxylic acid (0.91 g.), which can be represented as 2-(2-formylimino-5-chloro-2,3-dihydro-1,3-thiazol-4-yl)glyoxylic acid, mp. 148° to 152° C. (dec.). The remaining filtrate and washing were combined together and then extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and then the solvent was distilled off to give further the same object compound (0.23 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560765
Source datasetuspto-grants-1985_12
ORD IDord-0bbbf6224d0540069bfc5ef7daefb0e8
Source noteuspto-grants-1985_12