http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101863732-B
Outgoing Links
Predicate | Object |
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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 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C1-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C17-263 |
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 |
Incoming Links
Total number of triples: 69.