http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101768271-B

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2e39a288d149ab88e19e5b980e72fd1e
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G73-18
filingDate 2010-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4e9edc9879dd864c70eeb142b9ff52e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd3c0f6a43217652a0d2ce3309eb2f79
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_434a03947a6992e31742b6d4e2934649
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2ff8e1f2dc859fe3a8a451a34c790c00
publicationDate 2011-09-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101768271-B
titleOfInvention Method for protecting terminated amine in polybenzimidazole molecule by carbon dioxide
abstract Disclosed is a method for protecting terminated amine in a polybenzimidazole molecule by carbon dioxide, which is characterized in that polybenzimidazole is dissolved by a solvent, under the protection of nitrogen and action of catalyst, CO2 gas is input for reaction to generate the polybenzimidazole of which the terminated amine is protected, wherein, the solvent adopts dimethyl acetamide, dimethyl sulfoxide or N-methyl-pyrrolidone, and the catalyst adopts concentrated sulfuric acid, phosphoric acid, pyrophosphoric acid, polyphosphoric acid, solid superacid or a molecular sieve. The method is more stable than that using a carbonyl compound to generate Schiff alkali or using an acyl compound to generate amide; and is easier to perform than that using benzoic acid to protect reaction, excessive carbon dioxide can be added, and excessive carbon dioxide can be removed easily.
priorityDate 2010-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1381107-A2
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID466866974
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10332

Total number of triples: 18.