http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103819345-B
Outgoing Links
Predicate | Object |
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classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-84 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-45 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-50 |
filingDate | 2014-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2015-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2015-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-103819345-B |
titleOfInvention | A kind of preparation method of 2-aminobiphenyl derivate |
abstract | The invention discloses a kind of preparation method of 2-aminobiphenyl derivate, be specially and anils, phenylhydrazine derivant and phthalocyanine metal complex compound catalyzer are dissolved in solvent, react at 20-80 DEG C, obtain 2-aminobiphenyl derivate.The present invention uses anils for initiator, and raw material is easy to get, kind is a lot; The product types utilizing method of the present invention to obtain is various, not only directly can use, but also may be used for other and further react; Meanwhile, reaction conditions gentleness of the present invention, operation and last handling process are simple, and reaction process is catalysis, and greatly reduce the consumption of reagent and react generation and the discharge of refuse, productive rate is higher, is suitable for scale production. |
priorityDate | 2014-03-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 96.