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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-12
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N33-10
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C201-12
filingDate 2018-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fc01134e6eefcf2baeb29e64271d3631
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ea174f969900073434575a362e173c3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a900b55bb4c51e80684f40010bafe510
publicationDate 2019-01-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-109265350-A
titleOfInvention Synthesis method of acaricide diphenyl phthalate intermediate 3-nitro-4-methoxybiphenyl
abstract The invention relates to a method for synthesizing amidicide diphenyl phthalate intermediate 3 - nitro-4-methoxy phenyl, belonging to the field of pesticide pharmacy, characterized in that 4-halo- 2 nitroanisole and halobenzene Under the action of a catalyst, the reaction gives 3-nitro-4-methoxybiphenyl. The reaction process is as follows: 1) Mix 4-halogeno-2-nitroanisole, halogenated benzene, catalyst and solvent A under a protective gas condition, and raise the temperature to 130-150 ° C, and control the pressure to 7-12 At atmospheric pressure, the reaction ends at 20 to 35 hours; 2) the system is filtered under reduced pressure to remove solid insolubles to obtain filtrate a, and the filtrate a is poured into 3 to 5 volumes of water, and then solvent B is added for extraction, and the organic phase is separated after layering. The desiccant is dried and concentrated to give a solid, which is then recrystallized from solvent C to give 3 - nitro-4- methoxybiphenyl. The invention has fewer steps, higher yield and convenient operation.
priorityDate 2018-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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