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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1764131Erstellt: 23. Oktober 2026

Ethyl 2-bromooctanoate → Ethyl octanoate

https://huagongshe.com/de/reaction/1764131

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 2-bromooctanoateHCID 95580—
EduktSodiumHCID 5360545—
Eduktp-(1-Cyclooctenyl)-phenolHCID 53964233—
LösungsmittelEthanolHCID 702—
ProduktEthyl octanoateHCID 7799—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To 2.1 g of sodium in 150 ml of absolute ethanol are added with stirring 15 g of p-(1-cyclooctenyl)-phenol. After stirring has continued for a further 30 minutes, 30 g of 2-bromo-octanoic acid ethyl ester are slowly added dropwise to this solution and the mixture is maintained at 50° C for 24 hours. After the solvent has been removed in vacuo the residue is partitioned at 0° C between ether and 2N sodium hydroxide solutuion. The organic phase is washed until neutral, dried over sodium sulphate and evaporated in vacuo, to thus yield the oily α-[p-cyclooctenyl)-phenoxy]-octanoic acid ethyl ester of the formula ##STR9##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04115416
Quelldatensatzuspto-grants-1978_09
ORD IDord-afed50833532465593cb9c51a13384ba
Quellennotizuspto-grants-1978_09