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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_80fdaa0d94f29478467816f48d47639e
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C221-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C221-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C223-06
filingDate 2017-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0be20f0f2cd2cfe19a93a631f8c6ee8b
publicationDate 2018-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108395378-A
titleOfInvention A kind of synthetic method of pharmaceutical intermediate o-Aminobenzaldehyde
abstract A kind of synthetic method of pharmaceutical intermediate o-Aminobenzaldehyde, mainly includes the following steps:The o-nitrobenzaldehyde of 2mol is added in the reaction vessel, 50L water, the stannous chloride of 3 4mol, 2 amino toluenes of 5 6mol, 90-130rpm of control mixing speed, solution temperature is increased to 70-75 DEG C, 70-90min are reacted, 80-86 DEG C of fraction is collected in vacuum distillation, collect distillate, the potassium bromide of 1 2kg is added, reduces solution temperature to 5-8 DEG C, precipitates crystal, filtering, it is washed with dimethylamine solution, is washed with trifluoroacetic acid solution, dehydrating agent dehydration, it is recrystallized in ethane solution, obtains finished product.
priorityDate 2017-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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