http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2359819-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_567b1e0c9d5905537fc43cabba955532
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D201-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D201-04
filingDate 2009-11-13^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ab8e604ecb70174f132343bf2f082dab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fad3b23ffbdf699a4dddbe923978a9d3
publicationDate 2011-05-27^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2359819-A1
titleOfInvention PROCEDURE FOR OBTAINING E-CAPROLACTAMA FROM THE OXYM OF CICLOHEXANONA.
abstract Procedure for obtainingnε-caprolactam from the oxime ofncyclohexanonen n n The present invention relates to obtainingnε-caprolactam by reactionnBeckmann Transposition, by treating the oxime of thencyclohexanone with p-toluenesulfonyl chloriden(p-TsCl) using anion salts as catalystntosylate, and in particular tetramethylguanidinium tosylaten([TMG] [TsO]). This salt is also the subject of the present invention.nrequest. Ε-caprolactam is anlactam that through a chemical polycondensation reactionntransforms into the polyamide fiber calledn"nylon-6" Thenε-caprolactam is therefore the precursornDirect nylon 6.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2594501-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2016203069-A1
priorityDate 2009-11-13^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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