http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H02231474-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b9822bceff022feda91b10019125e70f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-89
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-287
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-63
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-04
filingDate 1988-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6640f4549d94fe47ea7a9dad1ffd95bc
publicationDate 1990-09-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02231474-A
titleOfInvention Production of n-fluoro-2,3,4,5,6-pentachloro-pyridinium salt
abstract PURPOSE: To produce the title compound in high yield safely by reaction between pentachloropyridine, fluorine and a Brϕnsted acid or Lewis acid in an acidic lower perfluoro saturated fatty acid as a solvent. n CONSTITUTION: In a lower perfluoro saturated fatty acid such as trifluoro-aceteic acid or pentafluoropropionic acid, the reaction of penta-chloropyridine with fluorine and a Brϕnsted acid of the formula: XH (X is Breϕnsted acid radical) such as trifluoromethanesulfonic acid is effected to give N-fluoro-2,3,4,5,6- pentachloro-pyridinium salt of formula I. Instead of the Brϕnsted acid, a Lewis acid is used to effect the reaction to give N-fluoro-2,3-4,5,6-pentachloropyridinium salt of formula II. The product is useful as a reagent for introducing simultaneously a fluorine atom and an acyloxy group into the double bond in an alkene. n COPYRIGHT: (C)1990,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H07233097-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5336772-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0494770-B1
priorityDate 1988-12-27-04:00^^<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: 20.