Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl Bromide | HCID 6332 | — |
| Edukt | N,N-Diethyl-p-vinylphenethylamine | HCID 3015378 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-Vinylphenethylammonium bromide | HCID 20554599 | — |
Reaktionsschritte
All the procedures were conducted in a dry nitrogen atmosphere since the product was extremely hygroscopic. In a 100 ml two necked flask equipped with a three way cock 8.6 g of the p-diethylaminoethylstyrene as obtained in Synthesis 1 were dissolved in 35 ml of absolute methanol and then 12.7 ml of ethyl bromide were injected via a syringe. The quaternization was completed after 48 hours at 40° C. without any side reactions. After the reaction mixture was concentrated under reduced pressure, 100 ml of ethyl acetate were injected via a syringe to immediately precipitate white crystals. The crystals thus formed were separated from the solution by filtration under a dry nitrogen atmosphere, washed with ethyl acetate, dried in vacuum and recrystallized from methanol-ethyl acetate solution. The results of elemental analysis of the crystals are as follows;
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04311799 |
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| Quelldatensatz | uspto-grants-1982_01 |
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| ORD ID | ord-b152447a8ebb427e9a412968d72c6538 |
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| Quellennotiz | uspto-grants-1982_01 |
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