Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583357Generated: November 1, 2026

Imidazole → 5-[2-(1-Imidazolyl)ethoxy]benzo[b]thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1583357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant5-(2-Chloroethoxy)benzo[b]thiophene-2-carboxylic acid methyl esterHCID 13663000—
SolventDimethylformamideHCID 6228—
Product5-[2-(1-Imidazolyl)ethoxy]benzo[b]thiophene-2-carboxylic acid methyl esterHCID 1366301633.1%

Reaction Steps

Sodium hydride (0.22 g. of 50% dispersion in mineral oil) was added portionwise with stirring to a solution of imidazole (0.306 g.) in dry N,N-dimethylformamide (10 ml.) and the mixture was stirred at room temperature for 30 minutes and then warmed for a few minutes. 5-(2-Chloroethoxy)benzo[b]thiophene-2-carboxylic acid methyl ester (1.22 g.) was then added and the mixture was heated on a steam bath for 5 hours, and then cooled and poured into water. The mixture was extracted several times with ethyl acetate and the combined extracts were washed well with water and dried (Na2SO4). Evaporation of the solvent gave an oil which was chromatographed on silica gel. Elution with chloroform gave first mineral oil and some impurity followed by pure product. The product containing fractions were evaporated to give a solid which was crystallized from ethyl acetate/petrol (b.p. 60°-80°) to give 5-[2-(1-imidazolyl)ethoxy]benzo[b]thiophene-2-carboxylic acid methyl ester (0.45 g.), m.p. 127°-129° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551468
Source datasetuspto-grants-1985_11
ORD IDord-0df336bb145f432e8a134a47c2b0ee3e
Source noteuspto-grants-1985_11