http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101479534-B1
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C205-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C205-03 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-03 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J19-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C201-06 |
| filingDate | 2012-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2015-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2015-01-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-101479534-B1 |
| titleOfInvention | Process of Preparing Dinitro Derivatives Using Photo-stimulation and Apparatus for Preparing the Same |
| abstract | A method for synthesizing a dinitro derivative using photo-impact and a reaction apparatus therefor are disclosed. The reaction solution A is prepared by dissolving the metal chloride nitro compound monomer in the first solvent. The halogenated nitro compound monomer is dissolved in a second solvent to prepare a reaction solution B. The reaction solution A and the reaction solution B are mixed so that the molar ratio of the monomers is in the range of 0.8: 1.0 to 1.0: 1.2, and the third solvent is added. The mixture is refluxed while light impact is applied to synthesize a dinitro derivative. Dinitro derivatives can be synthesized with high yield within a short time and industrialization is easy. |
| priorityDate | 2012-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 43.