http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108238864-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ec25bbf427ec21164b2ac36aff33e940
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-27
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-255
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-27
filingDate 2017-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bb791bb3af43755f6194362485bfd49
publicationDate 2018-07-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108238864-A
titleOfInvention The synthetic method of antiarrhythmic drug intermediate 1- (2,6- dimethoxys) -2- acetone
abstract The invention discloses the synthetic methods of antiarrhythmic drug intermediate 1 (2,6 dimethoxy) 2 acetone, include the following steps:1 (2,6 dimethyl, 3 hydroxyphenoxy) 2 aminopropanes are added in reaction vessel, potassium nitrate solution controls mixing speed, increases solution temperature, adds in BBP(Butyl Benzyl Phthalate solution, the reaction was continued;Dicyclopentadienyl vanadium dichloride is added in, metabisulfite solution reduces temperature, stands, solution is layered, and is separated oil reservoir, is washed with sulfur hexafluoride solution, the washing of 2 chlorobenzene phenol solutions, it is recrystallized in chloromethanes solution, dehydrating agent dehydration obtains finished product 1 (2,6 dimethoxy) 2 acetone.
priorityDate 2017-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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