| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D261-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D413-06 |
| classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D261-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-06 |
| filingDate |
2011-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5e5de4173e4df086431da935b70b09ed
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f8be8d73b9b9bda9734e258659497a6c |
| publicationDate |
2012-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
JP-2012111745-A |
| titleOfInvention |
5-trifluoromethyl-4-nitro-2-isoxazoline compound and method for producing the same |
| abstract |
A method for producing a 5-trifluoromethyl-4-nitro-2-isoxazoline compound by a direct trifluoromethylation method and the compound are provided. A 4-nitro-2-isoxazole compound and (trifluoromethyl) trimethylsilane are reacted in a solution, preferably in the presence of a phase transfer catalyst and a base, and if necessary, an acid treatment after the reaction. To produce a 5-trifluoromethyl-4-nitro-2-isoxazoline compound. [Selection figure] None |
| priorityDate |
2010-11-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |