http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5586819-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G69-32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G69-00
filingDate 1978-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_526d0e0d6006d86a8339cf67ad600888
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f1040976573b5351b36198732ecb7a2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e51b8381dbd585c4c13d68150dc782ed
publicationDate 1980-07-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5586819-A
titleOfInvention Preparation of aromatic polyamide
abstract PURPOSE: To obtain the title polyamide useful as film materials, etc. in good operating efficiency, by reacting an aromatic diamine and an aromatic dicarboxylic dihalide in a nitrogen-containing organic solvent having a specific amount of 1,3-dimethyl-2-imidazolidinone. n CONSTITUTION: 30W80Vol% of 1,3-dimethyl-2-imidazolidinone is added to a nitrogen-containing organic solvent, e.g., N,N-dimethylacetamide, N-methyl-2-pyrrolidone. In the resulting solvent, an aromatic diamine, e.g., p-phenylenediamine, methyl p-phenylenediamine, 2,6-diaminonaphthylene, benzidine-sulfonic acid is reacted with an aromatic dicarboxylic dihalide, e.g., terephthaloyl dichloride, tetrachloroterephthaloyl dichloride at a temperature range of not higher than 60°C, preferably about 20W50°C under stirring and the reaction product is neutralized to give the desired polyamide. n COPYRIGHT: (C)1980,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5599922-A
priorityDate 1978-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 43.