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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 6-(4-Chlorobutyryl)-3,4-dihydrocarbostyril | HCID 12833516 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 6-(1-Ethylenedioxy-4-chlorobutyl)-3,4-dihydrocarbostyril | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05008274 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-91bed590b18443869671f054e4cea870 |
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| Source note | uspto-grants-1991_04 |
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