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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 579914Erstellt: 25. Oktober 2026

Monobenzone → p-Benzyloxy-(1-methylheptyloxy)benzene

https://huagongshe.com/reaction/579914

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMonobenzoneHCID 7638—
EduktSodium HydroxideHCID 14798—
Edukt(+)-2-OctanolHCID 2723888—
Eduktp-Toluenesulfonic acid 1-methylheptyl esterHCID 3912199—
LösungsmittelEthanolHCID 702—
Produktp-Benzyloxy-(1-methylheptyloxy)benzeneHCID 13878908—

Reaktionsschritte

p-Benzyloxyphenol (50 g), ethanol (150 ml) and 50% NaOH aqueous solution (25 g) were mixed with stirring, followed by pouring in the mixture, optically active 1-methylheptyl p-toluenesulfonate derived from S-(+)-2-octanol, heating the mixture under reflux for 4 hours, distilling off most of ethanol, extracting with toluene, washing with acid, alkali and water, drying, concentrating and purifying the concentrate according to column chromatography with activated alumina (150 g) to obtain oily p-benzyloxy-(1-methylheptyloxy)benzene (68.6 g), which was then subjected to hydrogenolysis with 5% Pd-C catalyst in ethanol, followed by removing the catalyst, concentrating the solution and subjecting the concentrate to vacuum distillation to obtain oily p-(1-methylheptyloxy)phenol (IIIa-2) (30.7 g) having a b.p. of 129°-130.5° C./0.5 Torr.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04751019
Quelldatensatzuspto-grants-1988_06
ORD IDord-9b2d367a034e4347893a65e31c228f54
Quellennotizuspto-grants-1988_06