Henkel Research Corporation

Henkel Kommanditgesellschaft Auf Aktien

Zucker-aktiengesellschaft Uelzen-braunschweig

Kenneth J Weese

Karlheinz Hill

Bert Gruber

James R Tucker

Arno Behr

Hans-Peter Mueller

Steven M Hoagland

Steven D Axt

Octyl ethers and octadienyl ethers of glucose, sucrose, are disclosed. Compositions comprised of a mixture of octyl ethers of glucose and sucrose and those containing octadienyl ethers of sugar acids are also disclosed.

Octyl ethers and octadienyl ethers

Octyl ethers and octadienyl ethers of glucose, sucrose, bisphenol A, 4-substituted-2,2,6,6-tetramethylpiperidines are disclosed. Compositions comprised of a mixture of octyl ethers of glucose and sucrose and those containing octadienyl ethers of sugar acids and ring-opened epoxidized octadienyl ethers are also disclosed as are telomerization processes.

Telomerization of 1,3-butadiene

Alkadienyl ethers are prepared by the telomerization of conjugated dienes with polyols by continuous addition of the alkadiene to a reaction mixtue comprised of the polyol, secondary alcohol solvent, a portion of the alkadiene to be added, and low palladium catalyst concentration.

Telomerization process of a conjugated alkadiene with a polyol

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Daly City, CA, United States of America

Kenneth J Weese