Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 1-(3,3-Dimethylcyclohexyl)ethanone | HCID 91388 | — |
| Katalysator | Trioctylmethylammonium chloride | HCID 21218 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(3,3-Dimethylcyclohexyl)ethanone | HCID 91388 | — |
| Produkt | 1-Acetyl-3,3-dimethyl-1-(2-methyl-2-propenyl)cyclohexane | HCID 20384605 | — |
| Produkt | 3,3-Dimethyl-1-(2-methallyl-5-methyl-4-pentenoyl)cyclohexane | HCID 54015233 | — |
Reaktionsschritte
A slurry of 1-acetyl-3,3-dimethylcyclohexane (624 grams, 4 moles), granular sodium hydroxide (240 grams, 6 moles), Aliqu t® 336 (tricaprylmethylammonium chloride [35 grams]), methallyl chloride (432 grams, 4.8 moles), and 400 ml of toluene is heated at reflux for 4 1/4 hours. At the end of this time, one liter of water is added to the cooled reaction mass. The aqueous layer is discarded, and the organic layer is distilled rapidly through a short column to afford 203 grams of recovered 1-acetyl-3,3-dimethylcyclohexane, 500 grams of 1-acetyl-3,3-dimethyl-1-methallylcyclohexane, and 73 grams of 3,3-dimethyl-1-(2-methallyl-5-methyl-4-pentenoyl)cyclohexane) (1°-4°, 3.0 mm Hg) containing 5% of 3,3-dimethyl-1-(4-methyl-4-pentenoyl). A portion of the latter compound is isolated by GLC chromatography (1 foot × 1/4 inch 80% SE-30 packed column; 200° C isothermal) and exhibits the following odor and flavor properties:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04081479 |
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| Quelldatensatz | uspto-grants-1978_03 |
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| ORD ID | ord-b784fa5cb6f04711aaaa75cc4ba440b5 |
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| Quellennotiz | uspto-grants-1978_03 |
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