Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenylacetaldehyde | HCID 998 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | Cyclohexane | HCID 8078 | — |
| Edukt | 2,3-Butanedithiol | HCID 548353 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-Benzyl-4,5-Dimethyl-1,3-Dithiolane | HCID 20398675 | — |
Reaktionsschritte
Into a 100 ml flask equipped with reflux condenser and magnetic stirring bar and hot plate equipped with magnetic stirring apparatus is placed 0.2 grams of para-toluenesulfonic acid, 5 ml cyclohexane and 6.1 grams (0.05 moles) of 2,3-butanedithiol. With stirring, over a period of 30 minutes, 6.0 grams (0.05 moles) of phenylacetaldehyde is added to the reaction mass. The reaction mass is then heated to reflux and refluxed for a period of 10 hours during which time water of formation is removed. After the 10 hour period, the reaction mass is cooled and transferred to a separatory funnel. The reaction mass is washed with one 50 ml portion of saturated sodium chloride, dried over anhydrous sodium sulfate and filtered. The resulting filtrate is then distilled on a Microvigreux column yielding the following four fractions:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04515968 |
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| Quelldatensatz | uspto-grants-1985_05 |
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| ORD ID | ord-be3009770ae34e7aa9fa1040ba40f2e6 |
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| Quellennotiz | uspto-grants-1985_05 |
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