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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_81a0287b9d80ac5a639ca855ef616b95
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-0016
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-159
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D323-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D305-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D323-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D305-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-159
filingDate 1996-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4190093208f35266e19ab87d03e88868
publicationDate 1997-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-9703105-A1
titleOfInvention Preparation of cyclic oligomers of substituted cyclic ethers
abstract A method of producing cyclic oligomers of substituted oxiranes and oxetanes involves the slow addition to a solution of the ether in a relatively polar organic solvent such as dichloromethane or dichloroethane, of a stable protonic acid such as HBF4 or a cationogenic species for example triethyloxonium tetrafluoroborate or an alcohol in conjunction with a stable Lewis acid such as boron trifluoride etherate. The cyclic oligomer product is isolated from other reaction products, in particular the straight chain oligomers, by extraction with a non-polar solvent, hexane being preferred. The cyclic products are effective plasticisers for polyether polymers, particularly where the cyclic ether is related to or even the same as the ether in the polymer since compatability of the materials is then very likely and separation out of plasticiser unlikely to occur.
priorityDate 1995-07-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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