http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2011130904-A

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C17-25
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C17-23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C21-18
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C17-25
filingDate 2009-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2013-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2011130904-A
titleOfInvention METHODS FOR PRODUCING 1,1-Dichloro-2,3,3,3-tetrafluoropropene and 2,3,3,3-tetrafluoropropene
abstract 1. The method of obtaining 1,1-dichloro-2,3,3,3-tetrafluoropropene, characterized by the introduction of a mixture of isomers of dichloropentafluoropropane, which contains 1,1-dichloro-2,2,3,3,3-pentafluoropropane, in contact with water with an alkali solution in the presence of a phase transfer catalyst, and thus selectively dehydrofluorinating only 1,1-dichloro-2,2,3,3,3-pentafluoropropane in the mixture. 2. The method of obtaining 1,1-dichloro-2,3,3,3-tetrafluoropropene according to claim 1, where the mixture of isomers of dichloropentafluoropropane contains, in addition to 1,1-dichloro-2,2,3,3,3-pentafluoropropane, at least least one isomer selected from 1,3-dichloro-1,2,2,3,3-pentafluoropropane, 2,2-dichloro-1,1,3,3,3-pentafluoropropane, 1,2-dichloro-1 , 2,3,3,3-pentafluoropropane and 2,3-dichloro-1,1,2,3,3-pentafluoropropane. 3. The method for producing 1,1-dichloro-2,3,3,3-tetrafluoropropene according to claim 1, wherein the content of 1,1-dichloro-2,2,3,3,3-pentafluoropropane in the mixture of dichloropentafluoropropane isomers is at most 99, 5 mol% 4. The method for producing 1,1-dichloro-2,3,3,3-tetrafluoropropene according to claim 1, wherein the concentration of the aqueous alkali solution is from 0.5 wt% to 40 mol%. 5. The method for producing 1,1-dichloro-2,3,3,3-tetrafluoropropene according to claim 1, wherein the temperature at which the mixture of isomers of dichloropentafluoropropane is brought into contact with an aqueous alkali solution in the presence of a phase transfer catalyst is from 0 to 80 ° C. .6. The method for producing 1,1-dichloro-2,3,3,3-tetrafluoropropene according to claim 1, wherein the temperature at which the mixture of isomers of dichloropentafluoropropane is brought into contact with an aqueous alkali solution in the presence of a phase transfer catalyst is from 0 to 25 ° C. .7. A method for producing 2,3,3,3-tetrafluoropropene, which includes the reaction of interaction of 1,1-dichloro-2,3,3,3-tetrafluoropropene obtained by the method as described in claim 1, with hydrogen in the presence of
priorityDate 2008-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415729598
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419642764
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415729600
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415729599
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419531920
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2776731
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID61111
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID62315
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415730386
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID61112
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415730419
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID61110
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10986936
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID62353
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425193155

Total number of triples: 30.