http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1604733-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a05eadea97eec51a457572c73ce586f4
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C01B21-084
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C01B21-084
filingDate 1988-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7a8107204d1d50d8bb7f607c3f12475
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb923c6c2ebf28ec0dfbdc22ccd35482
publicationDate 1990-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1604733-A1
titleOfInvention Method of producing nitrozonium salts
abstract The invention relates to methods for producing nitrosone salts of the general formula (NO N A N- , where A N- - BF 4 , CLO 4 , SO 3 F, SIF 6 n n n N = 1-2, which can be used in organic syntheses as active nitrosating and oxidizing reagents, as well as initiators of electrophilic reactions. The purpose of the invention is to expand the nomenclature and increase the yield of nitrozone salts produced while maintaining their high purity. To do this, at 0-15 ° C in the presence of a solvent, the reaction is carried out between nitrogen tetroxide and tertiary ammonium salts of the general formula [ALK 3 NH] N A N- , where ALK is methyl, ethyl, n-butyln n n A N- - BF 4 , CLO 4 , SO 3 F - , SIF 6 , N = 1-2. The solvent is selected from the group methylene chloride, chloroform, concentrated nitric acid, or a mixture thereof. The ammonium salts necessary for the synthesis are obtained by reacting tertiary amines with the corresponding acids. The purity of the nitrosone salts obtained reaches 99.85-99.9%, and the practical yield as compared with the prototype increases by 6-11%. 1 hp f-ly.
priorityDate 1988-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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