Basf Aktiengesellschaft

Basf Corporation

Jochen Houben

Alfred Oftring

Richard Baur

Stefan Birnbach

Johannes Perner

Jay G Otten

Dieter Stoeckigt

Hans-Ulrich Jaeger

Klaus Wulz

Josef Mueller

Ronald E Greenough

Substituted glucosides

A process for preparing an etherified polyoxyalkylene derivative of the formula ##STR1## wherein R.sup.1 and R.sup.4 are identical or different and are each independently C.sub.1 -C.sub.20 alkyl, C.sub.3 -C.sub.5 alkenyl, C.sub.6 -C.sub.20 aryl, C.sub.6 -C.sub.20 alkyl aryl, C.sub.6 -C.sub.20 cycloalkyl, and mixtures thereof, R.sup.2 and R.sup.3 are identical or different and independent of each other are H, CH.sub.3, CH.sub.3 CH.sub.2, and mixtures thereof, m, m' and n are identical or different and are each greater than or equal to zero, with the proviso that m+m'+n is from 3 to 300; by reacting a polyoxyalkylene compound of the formula.

Method for the preparation of methyl ethers of polyether polyols

Long-chain alkylglucosides are purified by extraction with water from reaction mixtures obtainable by reacting monosaccharides and alcohols of 8 or more carbon atoms or by transacetalating short-chain alkylglucosides with alcohols of 8 or more carbon atoms, adjusted to a pH above 6 in either case.

Purification of long-chain alkylglucosides

Etherified polyoxyalkylene derivatives of the formula ##STR1## where R.sup.1 is hydrogen, C.sub.1 -C.sub.20 -alkyl or C.sub.3 -C.sub.5 -alkenyl, R.sup.2 and R.sup.3 independently of one another are each hydrogen, methyl or ethyl, R.sup.4 is C.sub.1 -C.sub.4 -alkyl and m and n are identical or different and are each greater than or equal to 0, with the proviso that the sum of m and n is from 3 to 300, are prepared by reacting the corresponding hydroxyl-containing polyoxyalkylene derivative with a dialkyl sulfate in the presence of an alkali metal hydroxide by a process in which the reaction is carried out at from 20.degree. to 60.degree. C. in the presence of an aqueous solution of an alkali metal hydroxide, the concentration of alkali metal hydroxide during the entire duration of the reaction being not less than 35% by weight, based on the aqueous phase, and not less than 1 mole of dialkyl sulfate and not less than one mole of alkali metal hydroxide are used per mole equivalent of organic hydroxyl groups.

Etherification of polyoxyalkylene derivatives

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Ludwigshafen, Germany

Jochen Houben