Basf Aktiengesellschaft

Hans-Heinrich Bechtolsheimer

Helmut Wolf

Rolf Fikentscher

Johannes Perner

Rudi Widder

Wolf-Dieter Balzer

Karl-Heinz Beyer

Alfred Oftring

Gerhard Wolf

Dieter Hertel

Toni Dockner

Gabriele Iffland

Andreas Hohmann

Enrique Freudenberg

Georg Schuh

Beate Strecker

J&uuml;rgen Mohr

Peter Wittmer

Armin Brucker

Joachim Bader

Rudolf Alt

Stefan Martin

Hans-Martin Mugrauer

Hans Klink

Method for separating alkali metal ions from alkoxylates

Preparation of alkyl glycosides

Process for the preparation of N-alkanoyl-polyhydroxyalkylamines

Carbonyl halides of the general formula I ##STR1## where R is an organic radical of more than 7 carbon atoms and X is chlorine or bromine, are prepared by reacting carboxylic acids of the general formula II ##STR2## where R has the abovementioned meaning, with phosphorus chlorides or bromides by treating these reaction mixtures with carboxamide/hydrochloride or hydrobromide mixtures which are not homogeneously miscible with the carbonyl halides I and then separating off the carboxamide hydrochloride or hydrobromide phase.

Preparation of carbonyl halides of more than 7 carbon atoms

Acyloxybenzenesulfonic acids and their alkali metal and alkaline earth metal salts are prepared by sulfonation of phenol in the presence of a small amount of a complexing agent for the sulfonating agent SO.sub.3 or chlorosulfonic acid, followed by esterification and, if required, neutralization to give the alkali metal or alkaline earth metal salt.

Preparation of acyloxybenzenesulfonic acids and their alkali metal and

Acyloxybenzenesulfonic acids and their alkali metal and alkaline earth metal salts are prepared by a process comprising sulfonation of a phenyl ester in the presence or absence of a small amount of a complexing agent for the sulfonating agent SO.sub.3 or chlorosulfonic acid, subsequent acylation and, if desired, neutralization to give the alkali metal or alkaline earth metal salt, and, if required, subjecting the latter to oxidative bleaching before drying.

Alkali metal and alkaline earth metal salts of acyloxybenzenesulfonic acids of the formula I ##STR1## where R is a saturated or unsaturated alkyl radical of 1 to 17 carbon atoms or is phenyl which is unsubstituted or monosubstituted or disubstituted by alkyl of 1 to 3 carbon atoms, halogen, methoxy or nitro, are prepared by neutralization, by a method in which a liquid acyloxybenzenesulfonic acid of the formula I and an aqueous solution of an alkali metal or alkaline earth metal hydroxide, carbonate or bicarbonate are combined in water, at from 0.degree. to 60.degree. C. and while mixing thoroughly, so that the pH is kept at from 2.5 to 7.0, and, if desired, the resulting salt is isolated from the aqueous solution in a conventional manner.

Preparation of alkali metal and alkaline earth metal salts of

Alkali metal and alkaline earth metal salts of acyloxybenzenesulfonic acids of the formula I ##STR1## where R is a saturated or unsaturated alkyl radical of 1 to 17 carbon atoms or is phenyl which is unsubstituted or monosubstituted or disubstituted by alkyl of 1 to 3 carbon atoms, halogen, methoxy or nitro, are prepared by neutralization, by a method in which a liquid acyloxybenzenesulfonic acid of the formula I and an aqueous solution of an alkali metal or alkaline earth metal hydroxide, carbonate or bicarbonate are combined in water, at from 0.degree. to 60.degree. C. and while mixing throughly, so that the pH is kept at from 2.5 to 7.0, and, if desired, the resulting salt is isolated from the aqueous solution in a conventional manner.

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Dittelsheim-Hessloch, Germany

Hans-Heinrich Bechtolsheimer