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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085111Generated: October 25, 2026

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

https://huagongshe.com/reaction/1085111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodiumHCID 5360545—
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 hyfrogen 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 silicagel 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 numberUS05008274
Source datasetuspto-grants-1991_04
ORD IDord-91bed590b18443869671f054e4cea870
Source noteuspto-grants-1991_04