http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006169127-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_33dafb5bbc2ec47ebcb7becbbe60f704 |
classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C43-15 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C41-06 |
filingDate | 2004-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_385fa343c59f5f56d14686ef28591bb2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8326a14daf1f0ed43f82196bd6c1e965 |
publicationDate | 2006-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2006169127-A |
titleOfInvention | Method for producing ether compound |
abstract | PROBLEM TO BE SOLVED: To provide an industrially advantageous telomerization method for reacting a conjugated diene compound and an alcohol to obtain an alcohol addition product having high terminal position selectivity (linear selectivity) with high productivity. When carrying out a telomerization reaction of a conjugated diene compound and an alcohol, the reaction is carried out in the presence of a palladium compound, an isocyanide represented by the general formula (I) and a tertiary amine. R 1 NC (I) (In the formula, R 1 represents an optionally substituted tertiary alkyl group.) [Selection figure] None |
priorityDate | 2004-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 207.