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HRID 579914作成日:2026年10月27日

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

https://huagongshe.com/reaction/579914

反応式

関与物質

役割名称HCID仕込み量
反応物MonobenzoneHCID 7638—
反応物Sodium HydroxideHCID 14798—
反応物(+)-2-OctanolHCID 2723888—
反応物p-Toluenesulfonic acid 1-methylheptyl esterHCID 3912199—
溶媒EthanolHCID 702—
生成物p-Benzyloxy-(1-methylheptyloxy)benzeneHCID 13878908—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04751019
出典データセットuspto-grants-1988_06
ORD IDord-9b2d367a034e4347893a65e31c228f54
出典メモuspto-grants-1988_06