http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2494084-C2

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_f85b2a702941aa780f7ce337b5ed2228
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2603-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2603-74
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2527-1213
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2527-1206
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C5-2246
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J27-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C5-29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C13-615
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C13-615
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C5-29
filingDate 2009-05-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f37717b3df9aa0774a64d1dda2c4abce
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bab727614a4203e730881f5ffeea81d3
publicationDate 2013-09-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2494084-C2
titleOfInvention Method of producing adamantane
abstract FIELD: chemistry. n SUBSTANCE: invention relates to a method of producing adamantane (tricyclo[3.3.1.1 3.7 ]decane) via isomerisation in two steps using endo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.0 2.6 ]decane) or endo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.0 2.6 ]decane) and exo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.0 2.6 ]decane) as the starting substance. The method involves the following steps: using one HF catalyst or two catalysts from HF catalysts and BF 3 catalysts without a solvent, at the first step for isomerisation of endo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.0 2.6 ]decane) to exo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.0 2.6 ]decane); and using a HF catalyst and a BF 3 catalyst without a solvent at the second step for isomerisation of exo-tetrahydrodicyclopentadiene (tricyclo[5.2.1.0 2.6 ]decane) to adamantane (tricyclo[3.3.1.1 3.7 ]decane). The two-step isomerisation reaction takes place in a liquid phase, obtained in a reaction of a liquid-phase solution, and output of adamantane is controlled such that it is equal to or less than total solubility of adamantane in exo-tetrahydrodicyclopentadiene and solubility of adamantane in endo-tetrahydrodicyclopentadiene at the second isomerisation step. n EFFECT: use of the disclosed method enables to obtain adamantane without deposit thereof in form of a solid residue even without a solvent. n 12 cl, 5 ex, 1 dwg
priorityDate 2008-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008019201-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1201279-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2937211-A
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID414882835
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15600
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18984031
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419549337
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17795
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419509663
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID449668538
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419486926
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7647
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9238

Total number of triples: 36.