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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27181생성일: 2026년 10월 25일

1,2-Dimethoxyethane → Ethyl 2-(1-benzyl-5-methyl-4-imidazolyl)-4-oxotetrahydrothiophene

https://huagongshe.com/reaction/27181

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Ethyl ThioglycolateHCID 12185—
반응물Ethyl 3-(1-benzyl-5-methyl-4-imidazolyl)-2-propenoateHCID 54025209—
반응물ButyllithiumHCID 178418339—
용매HexaneHCID 8058—
생성물Ethyl 2-(1-benzyl-5-methyl-4-imidazolyl)-4-oxotetrahydrothiopheneHCID 86737180—

반응 단계

A solution of ethyl mercaptoacetate (7.45 g., 0.062 mole) in 59 ml. of dry 1,2-dimethoxyethane is cooled to 5° C. and n-butyl lithium (41.3 ml., 0.062 mole) in hexane is added dropwise over 1/2 hour under a nitrogen atmosphere. To this solution is added ethyl 3-(1-benzyl-5-methyl-4-imidazolyl)-2-propenoate (13.0 g., 0.0514 mole) in 50 ml. of 1,2-dimethoxyethane at 10° C. The mixture is stirred at 50°-55° C. for 6 hours and is left at room temperature overnight. The reaction mixture is cooled in ice and is diluted with 300 ml. of ether and filtered. The solid is dissolved in 100 ml. of water and is acidified with dilute hydrochloric acid. The mixture is made basic with sodium bicarbonate and is extracted with a mixture of chloroform and methylene chloride. The combined extracts are dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The product ethyl 2-[1-benzyl-5-methyl-4-imidazolyl]-4-oxotetrahydrothiophene-5-(and/or 3)-carboxylate is obtained as a brown viscous liquid (12.6 g.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04220654
출처 데이터셋uspto-grants-1980_09
ORD IDord-43635b8c0f004ae4ab0630f6b70e2e18
출처 메모uspto-grants-1980_09