http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002322102-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2f8cfa5aee4410611b5c562275c9f8e3 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-02 |
| filingDate | 2001-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc61188ec6d6fefc25a318c2d1128ea8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70ea1c7edf1c60509a8a200a2ec15efa |
| publicationDate | 2002-11-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2002322102-A |
| titleOfInvention | Method for producing unsaturated chain alcohol |
| abstract | PROBLEM TO BE SOLVED: To obtain a corresponding unsaturated chain alcohol at a high conversion and a high selectivity from an unsaturated chain aldehyde having a plurality of unsaturated bonds. SOLUTION: Unsaturation having a plurality of unsaturated bonds in the presence of a secondary alcohol and a catalyst containing at least one metal selected from Group 3, 4, 9, 9 and 13 metals of the periodic table. The formyl group of the chain aldehyde is selectively reduced to produce the corresponding unsaturated chain alcohol without reducing the unsaturated bond (carbon-carbon unsaturated bond). As the unsaturated aldehyde, C 5-12 alkadienal (such as 2,4-hexadienal) can be used. |
| priorityDate | 2001-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 121.