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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579914Generated: October 25, 2026

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

https://huagongshe.com/reaction/579914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMonobenzoneHCID 7638—
ReactantSodium HydroxideHCID 14798—
Reactant(+)-2-OctanolHCID 2723888—
Reactantp-Toluenesulfonic acid 1-methylheptyl esterHCID 3912199—
SolventEthanolHCID 702—
Productp-Benzyloxy-(1-methylheptyloxy)benzeneHCID 13878908—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04751019
Source datasetuspto-grants-1988_06
ORD IDord-9b2d367a034e4347893a65e31c228f54
Source noteuspto-grants-1988_06