http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4238420-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c4010f2b9823f3e997c2a2d5f9e60c0e |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-12 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-06 |
filingDate | 1979-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 1980-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a251b9da26e1f8f9a9a2b6cb8128dd62 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_389883d770b1532de7a3fc3600d63c26 |
publicationDate | 1980-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | US-4238420-A |
titleOfInvention | Production of hexanitrostilbene using inorganic buffers |
abstract | The yield of hexanitrostilbene from the reaction of 2,4,6-trinitrotoluene and an alkali metal or alkaline earth metal hypochlorite, in an aqueous organic solvent, is improved by adjusting the pH of the reaction mixture to within the range 9.5 to 11.0 and then maintaining the pH within that range by the addition of an inorganic buffer. The pH is preferably kept above 9.75, especially from 10 to 10.5. n In a preferred embodiment, 2,4,6-trinitrotoluene is contacted with aqueous sodium hypochlorite (containing from 4 to 10% (w/v chlorine) in tetrahydrofuran-methanol. After an initial reaction period of between 0.5 to 3 minutes, an inorganic acid, especially sulphuric or hydrochloric acid is added to the reaction mixture to bring its pH within the required range, and then an inorganic buffer, especially sodium carbonate-sodium bicarbonate, is added to maintain the pH within that range. The controlled reaction proceeds for 1 to 2 hours at -5° to 25° C., preferably 10° to 16° C. During this time the reaction mixture need not be stirred. This minimizes the break up of the solid product and facilitates the filtration and washing of the hexanitrostilbene. Well-known methods of isolation then afford hexanitrostilbene in yields of about 50%. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4626606-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103694122-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103694122-B http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4307258-A |
priorityDate | 1978-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 74.