Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dibenzyl | HCID 7647 | — |
| Edukt | Chlorosulfonic acid | HCID 24638 | — |
| Edukt | Bibenzyl-4,4'-disulfonyl chloride | HCID 13356858 | — |
| Edukt | 4-(2-Phenylethyl)benzene-1-sulfonyl chloride | HCID 20352472 | — |
| Produkt | 4-(2-Phenylethyl)benzene-1-sulfonic acid | HCID 22157804 | — |
Reaktionsschritte
Polybibenzyl sulfone homopolymers are prepared by heating bibenzyl- 4 -sulfonyl chloride in the presence of a catalytic amount of an anhydrous Lewis acid, or by using a stoichiometric mixture of bibenzyl and bibenzyl- 4,4' -disulfonyl chloride as hereinafter described. The preparation of the homopolymer first necessitates the synthesis of either the mono or di sulfonyl chloride derivative of bibenzyl. Bibenzyl- 4 -sulfonyl chloride may be prepared by a three step procedure by treating bibenzyl in solution with approximately equi molar quantities of chlorosulfonic acid to form bibenzyl- 4 -sulfonic acid followed by neutralization in an aqueous medium using sodium or barium hydroxide to yield the sodium or barium salt which is in turn treated in a solvent with an acid halide such as thionyl chloride to yield bibenzyl- 4 -sulfonyl chloride. Another suitable technique for the preparation of the monosulfonyl chloride derivative involves the treatment of the free sulfonic acid derivative of bibenzyl in a solvent with a complex of phosgene and a tertiary organic amide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04088683 |
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| Quelldatensatz | uspto-grants-1978_05 |
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| ORD ID | ord-f6b94669b0fd400a9ffc22a4ac8f6aa4 |
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| Quellennotiz | uspto-grants-1978_05 |
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