http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2672580-T3

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filingDate 2013-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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publicationDate 2018-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2672580-T3
titleOfInvention Manufacturing processes of bis (phthalimide) s and polyetherimides, and bis (phthalimide) s and polyetherimides formed therefrom
abstract Process for the manufacture of a bis(phthalimide) composition, the process comprising catalyzing the imidation of a substituted phthalic anhydride and an organic diamine with a catalyst, in the presence of a solvent, the catalyst being selected from among quaternary ammonium salts, salts of quaternary phosphonium, guanidinium salts, pyridinium salts, imidazolium salts, and combinations thereof; wherein the substituted phthalic anhydride has a formula **Formula** and the organic diamine has a formula H2N-R-NH2; to provide the bis(phthalimide) composition comprising a catalyst residue, and a bis(phthalimide) of the formula **Formula*+ wherein, in the formulas above, X is selected from fluorine, chlorine, bromine, iodine, nitro, and combinations thereof, and R is selected from an aromatic hydrocarbon group having 6 to 27 carbon atoms, a halogenated derivative thereof, a straight or branched chain alkylene group having 2 to 10 carbon atoms, a halogenated derivative thereof, a cycloalkylene group having 3 to 20 carbon atoms, a halogenated derivative thereof, -(C6H10)z-, where z is an integer from 1 to 4, an aromatic hydrocarbyl moiety having presents from 1 to 6 aromatic groups, and a divalent group of the formula**Formula** in which Q1 is a member selected from the group of a single bond, -O-, -S-, -C(O) -, -SO2-, -SO-, -CyH2y, where y is an integer from 1 to 5, and combinations thereof; wherein the conversion to the bis(phthalimide) is 99% complete, based on moles of substituted phthalic anhydride, in less than 6 hours, and wherein the bis(phthalimide) comprises less than or equal to 0.5 mole percent residual substituted phthalic anhydride, and less than or equal to 2 mole percent monoamine, based on the total moles of the substituted phthalic anhydride, the organic diamine, and a monofunctional reactant, if any. uses.
priorityDate 2012-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8398
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86740854
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419594273
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419519584
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419556587
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11375816
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID412218272
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9795249
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67553
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID170751
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67044
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54111426
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22352145
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426093128
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420553325
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415862943
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559516
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18374
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID88242746
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415757317
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421900324

Total number of triples: 308.