http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101863732-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bf92d875575171572a064ae367ca3431
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C57-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C11-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-353
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-042
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C21-22
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filingDate 2009-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31ebd75f52e1a5f8bb392b0d1fa71e19
publicationDate 2013-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101863732-B
titleOfInvention Synthesis method of end-group alkyne
abstract The invention relates to a synthesis method of end-group alkyne, which comprises the steps of: mixing solvent and lithium acetylide ethylenediamine; cooling the solution to -10 to 10 DEG C when the solution is clear, and then adding haloalkane into the cooled solution; leading the molar ratio between the lithium acetylide ethylenediamine and the haloalkane to be 1: 1-2: 1, and controlling the temperature to be -20 to 20 DEG C and the reaction time to be 0.5-5h; and finally, extracting, washing, distilling, collecting fraction with the boiling point close to that of the product, and obtaining a finished product. Compared with the prior art, the synthesis method has the advantages of simple method, convenient operation, high yield and the like.
priorityDate 2009-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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