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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-017
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-21
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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
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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

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