http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111116416-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-09
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-02
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C253-30
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-42
filingDate 2019-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-03-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-111116416-B
titleOfInvention Preparation method of beta-amino acrylonitrile compound
abstract The invention discloses a preparation method of beta-amino acrylonitrile compounds. It comprises the following steps: in a solvent, reacting beta-amino cyanoacrylate shown as a formula I under the action of a catalyst to obtain a beta-amino acrylonitrile compound shown as a formula II; wherein R is 1 Is C1-C12 alkyl, halogenated C1-C12 alkyl, C3-C12 cycloalkyl, C2-C12 alkenyl, C2-C12 alkynyl, aryl, substituted aryl, benzyl or substituted benzyl; r 2 Is hydrogen, halogen, hydroxyl, amino, cyano, nitro, C1-C12 alkyl or halogenated C1-C12 alkyl. The method has the characteristics of good stereoselectivity, high yield, simple preparation of the raw material beta-amino cyanoacrylate and the like, and has great practical value.
priorityDate 2019-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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