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HRID 27181作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/27181

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DimethoxyethaneHCID 8071—
反応物Ethyl ThioglycolateHCID 12185—
反応物Ethyl 3-(1-benzyl-5-methyl-4-imidazolyl)-2-propenoateHCID 54025209—
反応物ButyllithiumHCID 178418339—
溶媒HexaneHCID 8058—
生成物Ethyl 2-(1-benzyl-5-methyl-4-imidazolyl)-4-oxotetrahydrothiopheneHCID 86737180—

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04220654
出典データセットuspto-grants-1980_09
ORD IDord-43635b8c0f004ae4ab0630f6b70e2e18
出典メモuspto-grants-1980_09