Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 1-Phenyl-1H-indene | HCID 519674 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | Bis(3-phenyl-2-indenyl)methane | HCID 22508191 | 246,7% |
Reaktionsschritte
In a 500 mL flask equipped with magnetic stirring bar were introduced 4.46 g (0.023 moles) of 1-phenyl-indene, 0.35 g (0.0117 moles) of formalin and 0.88 g (0.0046 moles) of para-toluenesulphonic acid in 200 ml of toluene; the mixture was heated to 80° C. and was maintained under stirring for 6 hours at 80° C. Then the reaction was quenched with water/NaHCO3; the organic layer was separated, washed with water and brought to dryness under reduced pressure. The crude product was crystallized upon standing at room temperature, and then was further purified by washing with pentane or MeOH, thus isolating 4.5 g of bis(3-phenyl-2-indenyl)methane (purity of 97.3% by G.C.; yield=95.2%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06872863B2 |
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| Quelldatensatz | uspto-grants-2005_03 |
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| ORD ID | ord-2637fa600f7a46f2855c676231b5e3fc |
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| Quellennotiz | uspto-grants-2005_03 |
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