Polyhydroxyl compounds containing acyl urea groups

Abstract

Abstract New polyols modified by acyl urea groups, process for the preparation thereof and use thereof as starting component for the preparation of preferably foamed polyurethane plastics. The process involves (A) reacting diisocyanatocarbodiimides corresponding to : OCN--R.sup.2 --N═C═N .sub.M --R.sup.2 --NCO with polyhydroxyl compounds corresponding to: A--OH).sub.n to form a polyhydroxyl compound containing carbodiimide groups and (B) completely or partially reacting, the carbodiimide groups remaining in the product of step (A), with a carboxylic acid corresponding to the following general formula: ##STR1## to form acyl urea groups, and (C) distilling off the inert solvent, if used; wherein m represents a number of from 1 to 10; s represents an integer of from 1 to 3; and R 1 represents hydrogen or a monofunctional or--in the form of a bridge to further acyl groups--a di- or trifunctional C 1 -C 18 aliphatic, C 4 -C 15 cycloaliphatic, C 6 -C 15 araliphatic or aromatic radical which may contain one or two double bonds and/or be branched and which may optionally contain one or two substituents selected from the group consisting of hydroxyl, mercapto, secondary amino, sulphonic acid ester, phosphonic acid ester, carboxylic ester, siloxane or trifluoromethyl groups, fluorine, chlorine, bromine or iodine; R 2 represents a difunctional aliphatic, cycloaliphatic, aromatic or araliphatic radical containing from 4 to 25 carbon atoms obtained by removing the isocyanate groups from a diisocyanate; A represents an n-functional radical obtained by removing the hydroxyl groups from a polyhydroxyl compound having a molecular weight of from 62 to 6000; X and Y, which may be the same or different, each represents oxygen or sulphur; N represents an integer of from 2 to 8.

Inventors

• 👤 Walter Schafer
• 👤 Kuno Wagner
• 👤 Kurt Findeisen

Bibliographic Details