http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2018177670-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02E60-10
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01M6-16
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01M10-0567
filingDate 2017-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f04c99d01b22790b068b404f8dfe2151
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7dd5312278411d659b1b2230935968b8
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publicationDate 2018-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2018177670-A
titleOfInvention Method for producing asymmetric imide tertiary ammonium salt
abstract The present invention provides a method for producing an asymmetric imide tertiary ammonium salt with high selectivity from the corresponding phosphoric acid amide and the corresponding sulfonyl halide. SOLUTION: The preparation of an asymmetric imide tertiary ammonium salt represented by the formula (1), wherein a phosphoric acid amide represented by the formula (2) and a sulfonyl halide represented by the formula (3) are reacted in the presence of an organic base. Method. [R 1 and R 2 are each independently a halogen group, an alkyl group, an alkoxy group, etc .; at least one of R 2 in the formula (3) is a halogen group; R 3 is a trimethylsilyl group or H; n is 1 or 2; M 1 n + is a tertiary ammonium cation] [Selected figure] Figure 1
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priorityDate 2017-04-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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