http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103787903-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_4dd5961a298aa39d55193ba3ca97a932
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-363
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C53-19
filingDate 2014-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8e7ba271978cacea9c820a5b5ca9e30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5c78a2bf7a4eb67b8e51890f8996fc39
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a84daa42774e34855fa91d0da3c89fe0
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_867f7393234deb092f5a5456e0759119
publicationDate 2014-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103787903-A
titleOfInvention A kind of method preparing levetiracetam intermediate 2-aminobutyric acid
abstract The invention discloses a method for preparing levetiracetam intermediate 2-aminobutyric acid represented by formula (III): firstly, in the first pipeline reactor, the raw material butyric acid is reacted with chlorine gas in the presence of a catalyst, Obtain the 2-chlorobutyric acid shown in formula (II); Then in the second pipeline reactor, 2-chlorobutyric acid is ammoniated in the presence of ammonium chloride and sodium hydroxide aqueous solution to obtain the formula (III) The 2-aminobutyric acid shown; the method of the present invention has high atom economy, few by-products, simple and convenient operation, and is suitable for industrial production.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109232236-A
priorityDate 2014-01-16-04:00^^<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: 25.