http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104945246-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C59-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-96
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-02
filingDate 2014-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_99678d3edac835273ef1d3a5f0531e6c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_66048d2515b9e8bc4658ac99d8a99f49
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publicationDate 2015-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-104945246-A
titleOfInvention A kind of preparation method of p-alkoxyphenylacetic acid and its intermediate
abstract The invention discloses a preparation method of p-alkoxyphenylacetic acid and its intermediate. The preparation method of p-alkylphenylacetic acid as shown in formula I disclosed by the present invention comprises the following steps: (1) in water, in the presence of alkali, the compound shown as formula II is hydrolyzed and ring-opened to form a salt; (2) After the reaction in step (1), the pH of the system is adjusted to 7-14, and the reaction system is directly subjected to a decarboxylation reaction of the compound shown in formula III under the action of an oxidizing agent. The preparation method of the compound shown in the formula II disclosed by the present invention comprises the following steps: performing condensation reaction of the compound shown in the formula IV and hydantoin under the catalysis of an alcohol amine compound in water. The preparation method of the invention has high yield, high purity, mild reaction conditions, simple operation, environmental protection and is more suitable for industrial production.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-110627639-A
priorityDate 2014-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 30.