http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2313525-C1

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 2006-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9235fec7aac045e92f6b5760aa48dbca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9d3d584ca439f01b4d9061e8ee54e6f
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publicationDate 2007-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2313525-C1
titleOfInvention Method for preparing 2,3-dialkyl-1,10-phenanthrolines
abstract FIELD: organic chemistry and synthesis. n SUBSTANCE: invention relates to a method for synthesis of 2,3-dialkyl-1,10-phenanthrolines. Method involves interaction of 8-aminoquinoline with aliphatic aldehydes in the presence of terbium trichloride TbCl 3 x 6 H 2 O or terbium nitrate Tb(NO 3 ) 3 x 6 H 2 O as a crystal hydrate catalyst in the molar ratio 8-aminoquinaline : R-CH 2 CHO : Tb = 45:100:1.2, respectively, under atmosphere pressure, in the temperature range 20-100 0 C for 5-24 h in dimethylformamide (DMFA) medium as a solvent. Phenanthroline and its derivatives are used in analytical chemistry as indicators in oxidative-reductive reactions. n EFFECT: improved method of synthesis.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022166442-A1
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priorityDate 2006-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 37.