http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108299222-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_28b282d4e09fa83c1f67673795fd293b
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C231-02
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-25
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-43
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filingDate 2018-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd681c5a3b0deed1cf3cfd7f9b1da733
publicationDate 2018-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108299222-A
titleOfInvention The Synthetic Technology of 2-Amino-4-Acetamidoanisole
abstract The invention discloses a 2-amino-4-acetamidoanisole ( ) synthesis process. The present invention takes p-methoxyaniline as raw material, carries out partial acylation reaction with acetic anhydride, makes described p-acetamidoanisole ( ), and then carry out nitration reaction, the 2-nitro-4-acetamidoanisole ( ), under the action of Pd/C catalyst, the hydrogen source reduction preparation 2-amino-4-acetamidoanisole ( ). The synthesis process of the present invention has low energy consumption, low cost, less solid waste and waste liquid, environmental protection, simple operation, mild reaction conditions, high industrial safety factor, and the total yield of the target compound is above 85% (based on the initial reaction raw materials) ), the HPLC purity is above 99.0%, the yield of the target compound is high, the quality is good, and it is more suitable for industrial production.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113773222-B
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priorityDate 2018-03-09-04:00^^<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: 32.