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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a4461d7f4199f282dc81529d76def990
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C1-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C11-22
filingDate 2016-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b51d2681b6e853dcd1198bf077700e2
publicationDate 2017-01-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106278776-A
titleOfInvention A kind of synthetic method of terbinafine pharmaceutical intermediate tert-butyl acetylene
abstract nullA kind of synthetic method of terbinafine pharmaceutical intermediate tert-butyl acetylene,Comprise the steps: agitator is being installed、Thermometer、Dropping funnel、In the reaction vessel of condenser,Add bisulfite potassium solution 310ml,Hexane 300ml,Raise solution temperature to 90 95 DEG C,Control mixing speed at 150 170rpm,Dropping 1,1 diaminourea 3,3 dimethylbutane 0.73mol,Time for adding controls at 3 5h,Add hypochlorous acid phenyl ester 0.81 0.84mol,React 90 120min,Raise solution temperature to 110 115 DEG C,Continue reaction 3 5h,Reduce solution temperature to 10 15 DEG C,Separate out solid,Filter,Brine,Acetonitrile washs,Decompression distillation,Collect the fraction of 100 108 DEG C,Recrystallization in hexamethylene,Obtain crystals tert-butyl acetylene.
priorityDate 2015-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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