http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1174415-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-307
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-63
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-307
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-63
filingDate 2001-07-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2003-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f88578f6037e14ee433ae127273c7855
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2bba2f06bcea00daae2de16b625bf962
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2518dd06b0adf79a2917c0409c447260
publicationDate 2003-10-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1174415-B1
titleOfInvention High purity preparation of fluorinated 1,3-dicarbonyls using BDM (bis-fluoroxydifluoromethane)
abstract A process for providing an α-fluorinated-β-dicarbonyl includes electrophilically fluorinating a β-dicarbonyl with bis-fluoroxydifluoromethane in the presence of an acid to provide the α-monofluorinated-β-dicarbonyl. The acid is preferably hydrofluoric acid. Preferred β-dicarbonyls include methyl-3-oxopentanoate and ethyl-4,4,4-trifluoroacetoacetate. The process can limit radical impurity byproducts to no more than 4% in some cases, and less than 0.5% in other cases. Theoretical yields of 95% α-monofluorinated-β-dicarbonyl are possible in some cases.
priorityDate 2000-07-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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