http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107056688-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J23-892
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-61
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-61
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-89
filingDate 2017-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2020-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-107056688-B
titleOfInvention Preparation method of 2, 3-dichloropyridine
abstract The invention discloses a preparation method of 2, 3-dichloropyridine, which takes 2,3, 6-trichloropyridine as a raw material, hydrogen as a hydrogen source and Pd-Ni/SiO 2 As catalyst, hydrogen as hydrogen source in Pd-Ni/SiO 2 And in the presence of a catalyst and an acid-binding agent, carrying out catalytic hydrogenation reaction at the pressure of 2-4 MPa and the temperature of 50-120 ℃, and reacting for 8-20 h to obtain 2, 3-dichloropyridine. The conversion rate of the raw material is 93.4%, the selectivity of the product 2, 3-dichloropyridine is 89.2%, and the defects of more three wastes and low product yield in the traditional method are overcome. Reaction adopts SiO 2 Compared with the traditional Pd/C catalyst, the supported Pd-Ni bimetallic catalyst has the advantages of good stability, high selectivity, low Pd consumption and repeated application, greatly reduces the production cost and has higher industrial application value.
priorityDate 2017-01-05-04:00^^<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: 55.