http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109456200-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C253-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C253-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C209-48
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-27
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-51
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-48
filingDate 2018-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109456200-B
titleOfInvention Preparation method of m-xylylenediamine
abstract The invention provides a method for preparing m-xylylenediamine. In this process, metaxylene is converted to isophthalonitrile by ammoxidation. The resulting isophthalonitrile is extracted with N-alkylpyrazole. The m-phthalonitrile solution obtained by extraction is subjected to resin decarboxylation acid and then enters a hydrogenation reactor for hydrogenation reaction to obtain m-xylylenediamine reaction solution. Finally, the m-xylylenediamine with high purity (> 99.9%) is obtained by rectification and separation. The method has the characteristics of simple reaction flow, low energy consumption, simple operation, high m-xylylenediamine yield, high m-xylylenediamine purity and the like.
priorityDate 2018-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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