http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2079488-C1

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4888b7a7824a6329d1acfbdf416eb22d
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-51
filingDate 1995-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82a20daab5a64d39a099d04cf4293574
publicationDate 1997-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2079488-C1
titleOfInvention Method for synthesis of mono- and diphthalonitriles
abstract FIELD: organic chemistry and technology. SUBSTANCE: invention relates to carboxylic acid nitriles, in part, method of synthesis mono- and diphthalonitriles of the formula where: y - oxide or sulfide bridge; n = 1 or 2. At n = 1 Ar - aromatic radical where R - H, C(CH 3 ) 3 , Hal, COOH; at n = 2 Ar - divalent aromatic radical or where x - simple bond or bridges O, S, CO, SO 2 , CZ 2 , CZ(CZ 3 ), C(CZ 3 ) 2 ; z - H or Hal. Method of synthesis involves interaction of 4-nitrophthalonitrile with mono- and bis-phenols and thiophenols in the presence of K 2 CO 3 in 75% aqueous dimethylformamide at 40-95 C followed by reaction mixture cooling, filtration, filtrate distillation under decreased pressure and utilization of the regenerated solvent in the following syntheses, vat residue for staining and wood deresination. Synthesized compounds were used for synthesis di- and tetracarboxylic acids and the corresponding anhydrides, phthalocyanines, polyphthalocyanines, polyhexazocyclanes and polyimides. EFFECT: enhanced purity, decreased waste, improved ecology of process. 1 tbl
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2459803-C2
priorityDate 1995-01-30-04:00^^<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: 21.