http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102030713-A

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f68ddaa0ddd894016af217422d657c22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C1-26
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F15-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C1-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C15-107
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C13-28
filingDate 2010-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa2ec7b37086a7bf6201429f402fc77a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d3cb9083be9151dd76b250885ff5240
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_db7c79370bcb46ba6c94291b90cf0783
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_08c626a789ce62aba7870dbd7181a64d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ff39cd4fd39e5dbad0054d5a68e8fdf
publicationDate 2011-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102030713-A
titleOfInvention Bisphenol functionalization benzimidazole salt and ionic Fe (III) complex thereof
abstract The invention belongs to the field of ligands and complexes, particularly relating to a bisphenol functionalization benzimidazole salt and an ionic Fe (III) complex thereof. The bisphenol functionalization benzimidazole salt has the general formula of [(ArCH2NC6H4NCH2Ar)CH]X, wherein Ar=3,5-R-2-(OH)-C6H2, R is selected from one of tertiary butyl and methyl, and X is selected from one of chlorine and bromine. The ionic Fe (III) complex containing the bisphenol functionalization benzimidazole salt has the characteristics of simple synthesis method, high yield and the like, is solid at the room temperature and can have stable waiting points in the air, has extremely high catalytic activity on a cross coupling reaction between an aryl grignard reagent and inactivated primary and secondary alkyl halohydrocarbons containing beta-H, and also has good catalytic activity on a direct cross coupling reaction between the aryl halohydrocarbon and inactivated primary and secondary alkyl halohydrocarbons containing beta-H in the presence of magnesium metal.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102603806-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102603806-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102887923-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-7033289-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102887923-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2018203697-A
priorityDate 2010-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID466587274

Total number of triples: 27.