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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6c8d4dc7bd1a30d8fda907fceaeb4e69
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-82
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-08
filingDate 2003-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b510ec5e666e7a21a210023f60f330cf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_afc0756f5f839c8534886f1b10406e8f
publicationDate 2004-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2004339075-A
titleOfInvention Method for producing terephthalic acid diester
abstract An object of the present invention is to provide a method for esterifying terephthalic acid and a monohydric alcohol, in which the concentration of terephthalic acid in a reaction solution can be improved and the esterification reaction can be performed efficiently. . An esterification reaction is performed from terephthalic acid and a monohydric alcohol to produce a terephthalic acid diester. The esterification reaction is carried out in the presence of an organic solvent in which the solubility of terephthalic acid is higher than that of a monohydric alcohol. A method for producing a terephthalic acid diester, wherein the infinite dilution activity coefficient (γ value) of terephthalic acid in an organic solvent is a value smaller than the γ value of terephthalic acid in a monohydric alcohol. Is preferred. [Selection diagram] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113233977-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017508857-A
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priorityDate 2003-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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