http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103288658-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_65682d3e437c225d79b93953b4b26392
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-08
filingDate 2013-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f590a54dd1c4c32e9003b71e898e8db1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_48142b2a3e0baf09148889768cc60898
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6bdca3a578532478ba4e88df77dc5cf7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85b63c3b5c916371027b14bc73e018fd
publicationDate 2014-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103288658-B
titleOfInvention Polyfluoroalkyl diol and preparation method thereof
abstract The invention relates to polyfluoroalkyl diol and a preparation method thereof. The preparation method disclosed by the invention comprises the following steps: performing ring-opening addition reaction on polyethylene polyamine and glycidyl in a polar solvent to generate polyamine diol, then adding olefin-containing a fluoroalkyl terminal, and utilizing carbon-carbon double bonds of the olefin-containing the fluoroalkyl terminal and a primary amino group and a secondary amino group in the polyamine diol to performing addition reaction through addition reaction between carbon-carbon double bonds of the olefin-containing the fluoroalkyl terminal and a primary amino group and a secondary amino group in the polyamine diol so as to obtain the polyfluoroalkyl diol. The reaction is completed by adopting a one-pot method, the preparation process is simple and convenient, the reaction conditions are mild, byproducts are avoided, and the preparation method is suitable for industrial production. The obtained polyfluoroalkyl diol is an alcohol compound with 2 degrees of functionality, has the characteristics of high fluorine content and determined reactivity and can be used as a synthetic fluoroalkyl modified polyurethane chain extender.
priorityDate 2013-06-14-04:00^^<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: 47.