http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2003119159-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1f8713f6ace083308920724981592661 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_afea2aa6f1f892c1456cf7d7a8bc0242 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2-66 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C2-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C15-18 |
filingDate | 2001-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a41c4f3c2c35183bbfba7ee49998cca |
publicationDate | 2003-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2003119159-A |
titleOfInvention | Method for producing diarylalkane |
abstract | (57) [Summary] (Modifications) [PROBLEMS] To produce a diarylalkane by alkylating an aromatic compound with a styrene derivative in the presence of a specific synthetic porous crystalline substance. SOLUTION: For example, benzene, toluene, xylene, ethylbenzene and cumene are used as aromatic compounds. In addition, for example, styrene, methylstyrene, or the like is used as the styrene derivative. As the catalyst, a synthetic porous crystalline substance having a structure of ZSM-12 is used. Examples of product diarylalkanes are 1,1-diphenylethane, 1-phenyl-1-tolylethane, 1-phenyl-1- Xylylethane. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2013115372-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2012169372-A1 |
priorityDate | 2001-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 50.