http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S62215580-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_13acffa0e4ce30d3be128ccd86b384f6 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-12 |
| filingDate | 1986-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_578db5838d1734490d460c1de53b4c0c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d4cbbb1073ebd9f3e20a69a7b73256f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9385797dea0342512807866c44800437 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b64cd89aa61a330600a363384df10664 |
| publicationDate | 1987-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S62215580-A |
| titleOfInvention | Novel tetrahydropyranyl ether |
| abstract | NEW MATERIAL:1-(Tetrahydropyran-2-yloxy)-11-dodecene of formula I. n USE: A synthetic intermediate of 11-dodecenyl acetate, a major component of the sex pheromone of tea leaf folder (Homona magnanima DIAKONOFF). The use of the compound enables the large-amount production of the pheromone. n PREPARATION: Only one hydroxyl in 1,12-dodecanediol of formula II is halogenated according to a usual manner to give 12-halododecanol of formula III (X is halogen). The remaining hydroxyl is protected with a tetrahydropyranyl group to form 12-halo-1-(tetrahydropyran-2-yloxy)dodecane. The product is allowed to react with a base such as potassium t-butoxide in an organic solvent such as dimethyl sulfoxide at room temperature, when needed, at 0°C to the boiling point of the solvent to give the compound of formula I. n COPYRIGHT: (C)1987,JPO&Japio |
| priorityDate | 1986-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.