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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 262217Erstellt: 27. Oktober 2026

Diethyl Ether → 5-(alpha-Hydroxyundecyl)-3-phenylbenzofuran

https://huagongshe.com/reaction/262217

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktAmmonium ChlorideHCID 25517—
EduktMagnesiumHCID 5462224—
Edukt5-Bromo-3-phenyl-1-benzofuranHCID 20330164—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(alpha-Hydroxyundecyl)-3-phenylbenzofuranHCID 21320298—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 5.5 g. (0.02 mole) of 5-bromo-3-phenylbenzofuran in tetrahydrofuran is added 0.5 g. (0.02 mole) of magnesium, and the mixture is heated at its reflux temperature for three hours. After cooling to 0° C., 3.4 g. of undecyl aldehyde is added. After stirring for 30 minutes at room temperature, the solution is added to ammonium chloride solution. Evaporation provides a residue which is mixed with diethyl ether and water. The ether layer is separated, washed with saturated sodium chloride solution, dried and evaporated. The resulting oil is dissolved in carbon tetrachloride and eluted from a silica gel column with carbon tetrachloride, then with dichloromethane. The later fractions are evaporated to provide 5-(α-hydroxyundecyl)-3-phenylbenzofuran which is dissolved in dichloromethane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04153716
Quelldatensatzuspto-grants-1979_05
ORD IDord-c49d250a9e154af5b535095b9dcf3100
Quellennotizuspto-grants-1979_05