http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-100500650-C

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d40285e27f4ed83b8728b0d477404958
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-50
filingDate 2007-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b6666896808cd604ea754bc751094a22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_34d7e9dfbe2e040feebb32547a49b520
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_30653bc3cf498220db7d64455acfc45e
publicationDate 2009-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-100500650-C
titleOfInvention Chemical synthesis method for nitriles substance
abstract The invention discloses a chemical synthesizing method of nitrile material, which comprises the following steps: reacting di-(trichloromethyl)-carbonate and N, N-disubstituted amide in the organic solThe invention discloses a chemical synthesizing method of nitrile material, which comprises the following steps: reacting di-(trichloromethyl)-carbonate and N, N-disubstituted amide in the organic solvent under -5-5 deg.c to produce Vilsmeier; adding aldoxime to react under 0-120 deg.c for 2-60 min; separating and purifying to obtain the product; setting the mass putting content of aldoxime, di-(tvent under -5-5 deg.c to produce Vilsmeier; adding aldoxime to react under 0-120 deg.c for 2-60 min; separating and purifying to obtain the product; setting the mass putting content of aldoxime, di-(trichloromethyl)-carbonate and N, N-disubstituted amide at 3;0.5-2:1.5-6; improving receiving rate obviously; saving cost effectively. richloromethyl)-carbonate and N, N-disubstituted amide at 3;0.5-2:1.5-6; improving receiving rate obviously; saving cost effectively.
priorityDate 2007-02-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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