http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112851527-B

Outgoing Links

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-4075
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C209-325
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F9-4056
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C201-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-45
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-36
filingDate 2020-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2022-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2022-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-112851527-B
titleOfInvention The preparation method of m-aminophenylacetylene
abstract The invention discloses a preparation method of m-aminophenylacetylene, which belongs to the technical field of organic synthesis. The method uses m-nitroacetophenone as a raw material, reacts with triethyl phosphite under the action of a catalyst, and the m-nitroacetophenone is continuously converted into an enol form and condensed with triethyl phosphite to obtain a condensed ester; Condensed esters are easy to separate and have high purity. The ester generates m-nitrophenylacetylene under the action of a strong base, which is reduced to obtain m-aminophenylacetylene. Compared with the acetophenone chlorination method, the synthesis method does not need to use phosphorus oxychloride to change the oxygen of m-nitroacetophenone into chlorine, with little pollution and high purity (up to 98%), avoiding the high pollution of raw material reagents. It is easy to use, easy to operate, green and environmentally friendly, and can easily realize industrialized production.
priorityDate 2020-12-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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