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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 597304Erstellt: 26. Oktober 2026

Ethyl 5-bromovalerate → 5-[p-(1-Cyclooctenyl)-phenoxy]-pentanoic acid ethyl ester

https://huagongshe.com/reaction/597304

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 5-bromovalerateHCID 84580—
EduktSodiumHCID 5360545—
Eduktp-(1-Cyclooctenyl)-phenolHCID 53964233—
LösungsmittelEthanolHCID 702—
Produkt5-[p-(1-Cyclooctenyl)-phenoxy]-pentanoic acid ethyl esterHCID 54374579—

Reaktionsschritte

12 g of p-(1-cyclooctenyl)-phenol are first added to a solution of 1.7 g of sodium in 60 ml of absolute ethanol whilst stirring in an anhydrous atmosphere, and after 30 minutes 18.8 g of 5-bromopentanoic acid ethyl ester are added dropwise. After completion of the addition, the mixture is stirred for 15 hours at 70° C and is evaporated to dryness in vacuo. The evaporation residue is distributed between 3 times 150 ml of ether and twice 100 ml of water. The organic phases are combined, dried over sodium sulphate and evaporated in vacuo. Chromatography of the evaporation residue on silica gel with chloroform as the eluant gives 5-[p-(1-cyclooctenyl)-phenoxy]-pentanoic acid ethyl ester of boiling point 165° -170° C at 0.03 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04013708
Quelldatensatzuspto-grants-1977_03
ORD IDord-a3789e0bc05e4e07864f7cb6f1be5937
Quellennotizuspto-grants-1977_03