http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104447812-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C15-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C1-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F1-08 |
| filingDate | 2014-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104447812-B |
| titleOfInvention | Have and be catalyzed triazole-cupric perchlorate coordination compound to methylphenylboronic acid and preparation method thereof |
| abstract | The present invention relates to have and be catalyzed triazole cupric perchlorate coordination compound to methylphenylboronic acid and preparation method thereof, disclose one { [Cu (L)] (ClO 4 )·0.25H 2 The preparation method of O} (1) (L=4 (3 (4H 1,2,4 triazole 4 base) phenyl) 4H 1,2,4 triazole).It is to use " hydro-thermal method ", i.e. Cu (ClO 4 ) 2 With L 100 o C hydrothermal condition gets off to prepare this coordination compound.The present invention further discloses copper complex { [Cu (L)] (ClO 4 )·0.25H 2 O} (1) (L=4 (3 (4H 1,2,4 triazole 4 base) phenyl) 4H 1,2,4 triazole) is as the application in terms of the coupling reaction catalyst to methylphenylboronic acid. |
| priorityDate | 2014-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.