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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894748Generated: October 30, 2026

Hydrochloric Acid → 2-(2-Aminothiazol-4-yl)-2-benzyloxyiminoacetic acid

https://huagongshe.com/reaction/894748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(2-aminothiazol-4-yl)-2-benzyloxyiminoacetateHCID 54194304—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Aminothiazol-4-yl)-2-benzyloxyiminoacetic acidHCID 5417256336.2%

Reaction Steps

A mixture of ethyl 2-(2-aminothiazol-4-yl)-2-benzyloxyiminoacetate (syn isomer, 35 g.), 1 N aqueous sodium hydroxide (172 ml.), methanol (150 ml.) and tetrahydrofuran (150 ml.) was stirred at 35° to 40° C. for 9 hours and at room temperature for 12 hours. After adjusted the resultant solution to pH 6.5 with conc. hydrochloric acid, the solution was concentrated to about 2/3 volume of the initial. The concentrate was adjusted to pH 3.5 with conc. hydrochloric acid under ice cooling, and the precipitates were collected by filtration, washed with water and acetone in turn and then dried over phosphorus pentoxide under reduced pressure to give 2-(2-aminothiazol-4-yl)-2-benzyloxyiminoacetic acid (syn isomer, 11.5 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284631
Source datasetuspto-grants-1981_08
ORD IDord-a99336a492694495a8da835f191f4f1a
Source noteuspto-grants-1981_08