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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-42
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-42
filingDate 1991-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_88eea20b574c5f834929914565d39624
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49d631070886f2763ec3d0ec8cacff5f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_142b9dd9c4f943826b8d2aeece905faa
publicationDate 1994-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H0687848-A
titleOfInvention Process for producing halogenated 1,3-dioxolane and new product obtained
abstract (57) [Summary] (Modified) [Structure] Bis (fluorooxy) perfluoroalkane represented by the formula C (OF) 2 X 5 X 6 and the formula CX 1 X 2 = A halogenated olefin represented by CX 3 X 4 , The reaction is carried out at a temperature of 140 ° C. to + 60 ° C. to give a compound of the general formula (I) And a 1,3-dioxolane of the general formula (I). (Wherein, X 1 , X 2 , X 3 and X 4 are F, Cl, B r, I, CF 2 OSO 2 F, SO 2 F, C (O) F, H, C 1 to 5 - be a perhaloalkyl or alkyloxy perhaloalkyl group; X 5 and X 6 is F or CF 3) EFFECT The method, without the use of complex reaction reagent, halogenated 1, This is a one-step production method capable of producing 3-dioxolane in a stable yield.
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priorityDate 1990-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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