http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106928098-B

Outgoing Links

Predicate Object
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C273-1809
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C281-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C281-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C281-12
filingDate 2015-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2019-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106928098-B
titleOfInvention A kind of synthetic method of indoxacarb intermediate semicarbazone
abstract The invention discloses a kind of synthetic methods of indoxacarb intermediate semicarbazone, comprising the following steps: 4- trifluoro-methoxyaniline and isocyanates generate 4- Trifluoromethoxyphen-l urea under acetic acid effect;4- Trifluoromethoxyphen-l urea occurs hydrazinolysis in organic solvent with hydrazine hydrate and reacts generation 4- trifluoro-methoxyaniline base hydrazides;4- trifluoro-methoxyaniline base hydrazides and the chloro- 1,3- dihydro -2- hydroxyl -1- oxo -2H- indenes -2- carboxylate methyl ester of 5- in organic solvent, generate semicarbazone class compound under the action of catalyst.The method of the present invention isocyanates being industrially easy to get passes through a series of synthetic intermediate semicarbazone that is converted;This method disadvantage low with yield at high cost when not only having avoided noble metal as catalyst, but also the technological deficiency that ring-closure reaction yield can be overcome low do not use noxious material phosgene product also;The method of the present invention synthesizes indoxacarb Atom economy and yield is higher, and safety is good.
priorityDate 2015-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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