Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | HCID 12832659 | HCID 12832659 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 12832660 | HCID 12832660 | — |
Reaction Steps
To a solution (30 ml) of 6-(18-hydroxy-1-oxooctadecyl)-2,3-dimethoxy-5-methylphenol (1.4 g) in acetic acid are added 5% palladium-on-carbon (50% hydrate; 0.5 g) and 70% perchloric acid (0.05 ml), and catalytic reduction is carried out at ambient temperature under atmospheric pressure. After completion of the absorption of hydrogen, the catalyst is filtered off and the filtrate is concentrated under reduced pressure to give a colorless oil. The oil is dissolved in ether, the ether layer is washed with a 5% aqueous sodium bicarbonate solution and dried over anhydrous sodium sulfate, and the solvent is distilled off to give crude crystals. Recrystallization from hexane gives colorless needles of 6-(18-acetoxyoctadecyl)-2,3-dimethoxy-5-methylphenol (1.4 g). m.p. 53° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04436753 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-63b3898efeb640bf96323663f1315605 |
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| Source note | uspto-grants-1984_03 |
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