Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | Hexachlorocyclobutene | HCID 22504 | — |
| Edukt | Sulfur trioxide | HCID 24682 | — |
| Produkt | Hexachlorobutadiene | HCID 6901 | 4,3% |
Reaktionsschritte
In a 500 cc flask, 143.4 g of 21.4% strength fuming sulphuric acid (oleum) were poured onto 209.8 of 95.3% pure hexachlorocyclobutene [199.9 g (0.766 mole) of hexachlorocyclobutene; remainder hexachloro-1,3-butadiene], with stirring (molar ratio of hexachlorocyclobutene:sulphuric acid:sulphur trioxide=1:1.5:0.5). The mixture was heated at 80° C. for 5 hours. After cooling, the reaction product was poured slowly into a mixture of ice and sodium chloride, with vigorous stirring, and the organic phase was then separated immediately from the aqueous phase. A mixture of 83.2 g of tetrachlorocyclobutenone, 58.9 g of hexachlorocyclobutene and 8.6 g of hexachloro-1,3-butadiene was obtained. The selectivity of the reaction was thus 75% of theory with a conversion of 71% of theory.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04272633 |
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| Quelldatensatz | uspto-grants-1981_06 |
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| ORD ID | ord-2aefc9fd1d2b4cc19004975c6dc8b60a |
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| Quellennotiz | uspto-grants-1981_06 |
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