Pyrrolidone, Capryllactam and Laurolactam as new Monomers for Polyamide Fibers

Authors


  • From a lecture delivered at the meeting of the Plastics and Rubber Section of the Gesellschaft Deutscher Chemiker on April 9th, 1962, in Bad Nauheim (Germany).

Abstract

The industrial production of capryllactam (1-azacyclononan-2-one) and of laurolactam (1-azacyclotridecan-2-one) starts with cyclization of acetylene or butadeine to give cyclooctatetraene or cyclooctadiene, or cyclization of butadiene to give cyclododecatriene. Further steps are: oxidation of the cyclic hydrocarbon to the ketone, formation of the oxime, and rearrangement of the latter with sulfuric acid. Pyrrolidone can be prepared from acetylene and formaldehyde by way of butyrolactone. The behavior of the lactams during polycondensation is described and the properties of the resulting fibers are compared with those of the known polyamide fibers.

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