http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106316894-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d40285e27f4ed83b8728b0d477404958
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C303-40
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-16
filingDate 2015-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14c3717bde8f8b1498ce3024aa12ea2b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_80cd1b7870bafad91571d563143690c3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f521cf9342b023482f0b3a236a80d20a
publicationDate 2017-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106316894-A
titleOfInvention A kind of synthetic method of nitroacrylamide compounds
abstract The invention discloses a method for synthesizing nitroacrylamide compounds represented by formula II: adding acrylamide compounds represented by formula I, N-chlorosuccinimide, and AgNO 2 into an organic solvent, 25~ React at a temperature of 100° C. for 5 to 20 hours, and the resulting reaction liquid is separated and purified to obtain nitroacrylamide compounds represented by formula II. The invention has the advantages that the nitrogen source system is cheap and easy to obtain, has low toxicity, is environmentally friendly, has mild reaction conditions, has good functional group universality, is easy to operate, and the like.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113491790-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110540522-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110540522-B
priorityDate 2015-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID408781675
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID147626425

Total number of triples: 18.