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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 225353Erstellt: 25. Oktober 2026

Ethylene Glycol → 7-[3-(2-Hydroxyethoxy)-5-oxocyclopent-1-EN-1-YL]heptanoic acid

https://huagongshe.com/reaction/225353

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktMethanolHCID 887—
Edukt2,6-LutidineHCID 7937—
Edukt4-Bromo-2-(6-carboxyhexyl)cyclopent-2-en-1-oneHCID 13046277—
KatalysatorSilver tetrafluoroborateHCID 159722—
LösungsmittelWaterHCID 962—
Produkt7-[3-(2-Hydroxyethoxy)-5-oxocyclopent-1-EN-1-YL]heptanoic acidHCID 23329941—

Reaktionsschritte

To a stirred solution of 19.1 g. of crude 4-bromo-2-(6-carboxyhexyl)cyclopent-2-en-1-one (Example 8) in 310 ml. of ethylene glycol is added 15.6 g. (80 mmole) of silver fluoborate during 2 minutes. The exothermic reaction is controlled to give a temperature of 29° C., and after 1 minute the mixture is treated during 1 minute with 8.6 g. (λmmole) of 2,6-lutidine. The mixture is stirred at ambient temperature for 2 hours, diluted with water, and filtered. The filtrate is diluted with saturated sodium chloride solution and extracted with ether. The extract is washed with half-saturated sodium chloride solution containing a little hydrochloric acid and saturated sodium chloride solution. The extract is dried over magnesium sulfate and concentrated. Column chromatography of the residue on silica gel gives an oil, λmax.MeOH =216 mμ(8350); νmax.=3340 (hydroxyl groups), 1700 (carbonyl groups), and 1620 cm-1 (olefin group).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04236027
Quelldatensatzuspto-grants-1980_11
ORD IDord-60f3cfbf064447df9c0fc0c84d03b4c7
Quellennotizuspto-grants-1980_11