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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358472생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/358472

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Ethyl bromopyruvateHCID 66144—
반응물N,N-Dimethylaminothioacetamide hydrochlorideHCID 13121932—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물Ethyl 2-((dimethylamino)methyl)thiazole-4-carboxylateHCID 2039211—

반응 단계

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:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04468399
출처 데이터셋uspto-grants-1984_08
ORD IDord-d7cc5060a35a465399a53624fafdc06a
출처 메모uspto-grants-1984_08