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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 371966Erstellt: 23. Oktober 2026

Dibenzyl → 4-(2-Phenylethyl)benzene-1-sulfonic acid

https://huagongshe.com/de/reaction/371966

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDibenzylHCID 7647—
EduktChlorosulfonic acidHCID 24638—
EduktBibenzyl-4,4'-disulfonyl chlorideHCID 13356858—
Edukt4-(2-Phenylethyl)benzene-1-sulfonyl chlorideHCID 20352472—
Produkt4-(2-Phenylethyl)benzene-1-sulfonic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04088683
Quelldatensatzuspto-grants-1978_05
ORD IDord-f6b94669b0fd400a9ffc22a4ac8f6aa4
Quellennotizuspto-grants-1978_05