http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2081920-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P39-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-62
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-62
filingDate 2006-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6fc9053e7b522375464be77a501a665
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8921a4595ddeef454bcecd2f662bcf5f
publicationDate 2011-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2081920-B1
titleOfInvention Method for preparing 3-o-alkyl-ascorbic acid
abstract The present invention relates to a method for preparing 3- O- substituted ascorbic acid derivatives represented by formula 1, in which 5, 6-O-isopropylidene ascorbic acid is reacted with a halide in an organic solvent in the presence of the anion exchange resin absorbed with multi-iodine anions and then deprotected. The method of the present invention has an advantage of providing a target compound with high purity and high yield by finishing the reaction within a short period of time at room temperature.
priorityDate 2006-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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