関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Monobenzone | HCID 7638 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | (+)-2-Octanol | HCID 2723888 | — |
| 反応物 | p-Toluenesulfonic acid 1-methylheptyl ester | HCID 3912199 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | p-Benzyloxy-(1-methylheptyloxy)benzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04751019 |
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| 出典データセット | uspto-grants-1988_06 |
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| ORD ID | ord-9b2d367a034e4347893a65e31c228f54 |
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| 出典メモ | uspto-grants-1988_06 |
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