Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27181Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantEthyl ThioglycolateHCID 12185—
ReactantEthyl 3-(1-benzyl-5-methyl-4-imidazolyl)-2-propenoateHCID 54025209—
ReactantButyllithiumHCID 178418339—
SolventHexaneHCID 8058—
ProductEthyl 2-(1-benzyl-5-methyl-4-imidazolyl)-4-oxotetrahydrothiopheneHCID 86737180—

Reaction Steps

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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220654
Source datasetuspto-grants-1980_09
ORD IDord-43635b8c0f004ae4ab0630f6b70e2e18
Source noteuspto-grants-1980_09