HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579914Generated: October 25, 2026
Monobenzone → p-Benzyloxy-(1-methylheptyloxy)benzene
https://huagongshe.com/reaction/579914
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Monobenzone | HCID 7638 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (+)-2-Octanol | HCID 2723888 | — |
| Reactant | p-Toluenesulfonic acid 1-methylheptyl ester | HCID 3912199 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | p-Benzyloxy-(1-methylheptyloxy)benzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04751019 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-9b2d367a034e4347893a65e31c228f54 |
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| Source note | uspto-grants-1988_06 |
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