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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200236Generated: November 1, 2026

Ethanol → Ethyl 2-((dimethylamino)methyl)thiazole-4-carboxylate

https://huagongshe.com/reaction/1200236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl bromopyruvateHCID 66144—
ReactantN,N-Dimethylaminothioacetamide hydrochlorideHCID 13121932—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductEthyl 2-((dimethylamino)methyl)thiazole-4-carboxylateHCID 2039211—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A reaction mixture was prepared containing 15.5 g. of dimethylaminothioacetamide hydrochloride, 20.5 g. of ethyl bromopyruvate and 100 ml. of ethanol. The reaction mixture was heated to refluxing temperature for about four hours after which time the solvent was removed in vacuo in a rotary evaporator. The residue, containing ethyl 2-dimethylaminomethyl-4-thiazolecarboxylate formed in the above reaction, was dissolved in a mixture of ether and water. The aqueous layer was separated. The ether layer was extracted with an equal volume of water and then discarded. The two aqueous layers were combined and washed with ether. The ether layer was again discarded and the aqueous layer cooled to a temperature in the range of 0-5° C. Solid potassium carbonate was added until the aqueous layer gave a basic reaction to litmus. An oil separated comprising ethyl 2-dimethylaminomethyl-4-thiazolecarboxylate free base. The oily layer was extracted with ether and the ether extract separated and dried. The ether was removed by evaporation in vacuo. The resulting residue was purified by gradient high pressure liquid chromatography (silica ethyl acetate). Ethyl 2-dimethylaminomethyl-4-thiazolecarboxylate thus obtained had the following physical characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04904792
Source datasetuspto-grants-1990_02
ORD IDord-9df6c243f3254bdfb8e50fd4dfd97c70
Source noteuspto-grants-1990_02