http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108586280-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-562
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C241-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-22
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C243-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C241-04
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C47-198
filingDate 2017-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2020-11-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108586280-B
titleOfInvention Method for synthesizing N' - [ (2S,3S) -2- (benzyloxy) pentan-3-yl ] formylhydrazine
abstract The invention discloses a method for synthesizing N' - [ (2S,3S) -2- (benzyloxy) pent-3-yl ] formhydrazide, which comprises the steps of reacting (S) -2-benzyloxy propionic acid with ethylenediamine to obtain (S) -2- (1-benzyloxy ethyl) -4, 5-dihydro-1H-imidazole; adding metal sodium into (S) -2- (1-benzyloxyethyl) -4, 5-dihydro-1H-imidazole under the protection of nitrogen, stirring and reacting to obtain (S) -2-benzyloxypropanal; reacting (S) -2-benzyloxy propionaldehyde with formylhydrazine, and carrying out post-treatment to obtain (S) -N' - (2-benzyloxy propylene) formylhydrazine; reacting (S) -N '- (2-benzyloxy propylene) formylhydrazine with a Grignard reagent, and carrying out post-treatment after the reaction is finished to obtain the product N' - [ (2S,3S) -2- (benzyloxy) pentan-3-yl ] formylhydrazine. Has the advantages of no use of expensive and unsafe organic aluminum compound, low preparation cost, simple post-treatment and simple and convenient operation.
priorityDate 2017-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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