VERFAHREN ZUR HERSTELLUNG VON (ALPHA)-STAENDIG SULFONIERTEN,(ALPHA),(BETA)-UNGESAETTIGTEN CARBONSAEUREALKYLESTERN SOWIE DANACH ERHAELTLICHE VERBINDUNGEN

VERFAHREN ZUR HERSTELLUNG VON (ALPHA)-STAENDIG SULFONIERTEN,(ALPHA),(BETA)-UNGESAETTIGTEN CARBONSAEUREALKYLESTERN SOWIE DANACH ERHAELTLICHE VERBINDUNGEN

The title compounds are obtained by reacting compounds corresponding to the following formula: R1-CH=CH-CO2R2 wherein R1 represents hydrogen or a methyl group and R2 represents a primary or secondary C1 to C4 alkyl group, with from 0.6 to 1.6 mol. equivalents of SO3 and, optionally, with from 0.1 to...

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Bibliographische Detailangaben
Hauptverfasser: NEUKAM,THEO,.DR, BRAEUER,WOLFGANG,.DR, KORTE,SIEGFRIED,.DR
Format: Patent
Sprache:ger
Schlagworte:
ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
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Zusammenfassung:The title compounds are obtained by reacting compounds corresponding to the following formula: R1-CH=CH-CO2R2 wherein R1 represents hydrogen or a methyl group and R2 represents a primary or secondary C1 to C4 alkyl group, with from 0.6 to 1.6 mol. equivalents of SO3 and, optionally, with from 0.1 to 10 mol. equivalents of an alkylating agent at temperatures in the range from -10 DEG to +25 DEG C., subsequently heating the resulting reaction mixture for 0.5 to 6 hours to 70 DEG -200 DEG C. and then working it up by distillation.