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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647734Generated: October 30, 2026

Ethylene Glycol → 6-(1-Ethylenedioxy-4-chlorobutyl)-3,4-dihydrocarbostyril

https://huagongshe.com/reaction/1647734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium BicarbonateHCID 516892—
Reactant6-(4-Chlorobutyryl)-3,4-dihydrocarbostyrilHCID 12833516—
SolventBenzeneHCID 241—
Product6-(1-Ethylenedioxy-4-chlorobutyl)-3,4-dihydrocarbostyrilHCID 131716824—

Reaction Steps

10 Grams (39.7 mM) of 6-(4-chlorobutyryl)-3,4-dihydrocarbostyril was dissolved in 300 ml of benzene, then to this solution was added 7.4 g (120 mM) of ethylene glycol and 300 mg of p-toluenesulfonic acid, and the whole mixture was refluxed by heating under dehydrating in Dean-Stark extractor for 6 hours. The reaction mixture was cooled and neutralized with an aqueous solution saturated with sodium hydrogen carbonate, then extracted with chloroform. The chloroform extract was washed with water then dried with anhydrous magnesium sulfate, then concentrated by removing the solvent by evaporation. The residue thus obtained was purified by means of a silica-gel column chromatography (eluent: chloroform:methanol=40:1) to yield 10.5 g of 6-(1-ethylenedioxy-4-chlorobutyl)-3,4-dihydrocarbostyril.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434164
Source datasetuspto-grants-1995_07
ORD IDord-e01c1816c81341248d9317c2c80a5800
Source noteuspto-grants-1995_07