http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100928055-B1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2523-44
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C15-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J23-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C4-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C11-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C7-00
filingDate 2007-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2009-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100928055-B1
titleOfInvention Arylalkyne compound from dehydrogenation of propionic acid derivative by carbon dioxide reaction and its preparation method
abstract The present invention relates to a process for producing an arylalkyne compound, and more particularly, to a process for producing an arylalkyne compound efficiently using Sonogashira reaction and dehydrocarbonation reaction using a propiolic acid derivative in the same reaction vessel .n n n The arylalkyne compound according to the present invention is economical to the starting material because it is lower in cost than the alkyne compound of the protecting group, which has been widely used in the existing Sonogashira reaction using propionic acid, and the by- Carbon dioxide is generated, which is more environment friendly than conventional metal waste.n n n Arylalkyne, sonogashira, de-carbon dioxide, propiolic acid
priorityDate 2007-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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