http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20160098488-A

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filingDate 2014-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a4c57e1bda028fc1f1b8b7d990b7790f
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publicationDate 2016-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20160098488-A
titleOfInvention Enhanced regio-selectivity in glycol acylation
abstract A method of acid-catalyzed acylation of isohexides is described. The process involves the reaction of isohexides and excess carboxylic acids in the presence of a Lewis acid or a Bronsted acid catalyst. One or more Lewis acid and / or Bronsted acid can achieve a high conversion rate of isohexides to the corresponding mono and diesters having a much higher selectivity of exo- OH than the endo- OH of isohexides in the product have. Specific catalytic acid species include zirconium chloride (ZrCl 4 ) and phosphonic acid (H 3 PO 3 ), which exhibit a ratio of exo : endo reactivity of about 5: 1 and 4: 1, respectively.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20160143712-A
priorityDate 2013-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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