http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101781199-B
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d40285e27f4ed83b8728b0d477404958 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-584 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-582 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-017 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-21 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-78 |
filingDate | 2010-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2013-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2508decb9b8ff68e05e318a0ae9aa9e7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6aa82b2d0fdefef6b0f4a25c15b3a001 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d2f7484bd11280e85889398094738b22 |
publicationDate | 2013-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-101781199-B |
titleOfInvention | Chemical synthesis method of O-acylcalix[4]arene |
abstract | The invention relates to a chemical synthesis method of O-acylcalix[4]arene shown in the formula (I). The synthesis method comprises the following steps: dissolving the calixarene shown in the formula (II) in organic solvent, reacting with the acylation reagent shown in the formula (IV) at 0-150 DEG C for 0.1-10 hours under the catalysis of lithiumtrifluoromethanesulfonate shown in the formula (III), and reprocessing reaction liquid to obtain O-acylcalix[4]arene shown in the formula (I), wherein in the formula (I) and (II), R1 represents C1-C6 alkyl or hydrogen; in the formula (I) and (IV), R2 represents C1-C6 alkyl, phenyl or benzyl; and in the formula (IV), X is Cl or R2COO. The beneficial effects of the invention are as follows: the catalyst used in the reaction can be reused; the yield is high (generally over 80%); the process route is advanced, the reaction conditions are mild; and the amount of catalyst is small and the method is environmentally friendly. |
priorityDate | 2010-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 96.