http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103467303-B

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-07
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-00
filingDate 2013-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a3b326dcb0a5d2a68593457986b91a08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_804de4d3d8da3e9ffd0512a0a2bbe60c
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publicationDate 2015-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103467303-B
titleOfInvention Preparation method of 1, 3-dimethyl-pentylaminehydrochloride
abstract The invention discloses a preparation method of 1, 3-dimethyl-pentylaminehydrochloride. The preparation method comprises the following steps: performing condensation and dehydration on 2-methylbutyraldehyde used a starting material and nitroethane under the catalyzing of an acetic acid/ ethylenediamine composite catalyst in a methylbenzene solvent to obtain a nitroolefin compound; reducing through potassium borohydride or sodium borohydride; then reducing through palladium carbon and acidizing through hydrochloric acid to obtain 1, 3-dimethyl-pentylaminehydrochloride. The preparation method of 1, 3-dimethyl-pentylaminehydrochloride has the advantages that the raw materials are simple and easy to obtain; the reaction condition is mild; the total yield is high; the industrial production can be performed well.
priorityDate 2013-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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