http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105753760-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bac2bf5b7fc2212f3492dc92044145de
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-24
filingDate 2014-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f38990afc2837e42e53c73068aae3a83
publicationDate 2016-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105753760-A
titleOfInvention A synthetic method of a medical intermediate N-boc-3-pyrrolidinone
abstract The invention relates to a synthetic method of a medical intermediate N-boc-3-pyrrolidinone. The method adopts pyrrolidone as a raw material and includes ammoniating with butyrolactone under 1.5 atmospheric pressures at 150-170 DEG C under the action of a solvent that is ethanol to generate the N-boc-3-pyrrolidinone. The method is simple, efficient, safe in operation and particularly practical in practical production.
priorityDate 2014-12-20-04:00^^<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: 18.