1962-74-9Relevant articles and documents
Preparation method of terephthalic acid and diester thereof
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Paragraph 0036; 0038, (2017/06/23)
The invention discloses a preparation method of terephthalic acid and diester thereof. Specifically, under the action of a supported metal catalyst, 2-cyclohexene-1,4-dicarboxylic acid undergoes catalytic dehydro-aromatization in a polar solvent or a nonpolar solvent so as to prepare terephthalic acid and diester. The polar solvent is water, methanol, ethanol, n-propanol, isopropanol, n-butanol, glycol dimethyl ether and diglyme. The nonpolar solvent is one or more than two components selected from a group consisting of n-hexane, n-heptane, normal octane, cyclohexane, benzene and toluene. A metal active component of the supported metal catalyst is non-noble metal and/or noble metal. A carrier for the supported metal catalyst is one or more than two components selected from a group consisting of a carbon carrier, nanoscale metal oxide, nanometer nonmetal oxide and a molecular sieve. When conversion rate of 2-cyclohexene-1,4-dicarboxylic acid is 95% and above, selectivity of terephthalic acid or diester of terephthalic acid can reach 90%.
Preparation of monoalkyl terephthalates: An overview
Chenot, Elodie-Denise,Bernardi, Dan,Comel, Alain,Kirsch, Gilbert
, p. 483 - 490 (2007/10/03)
Terephthalic acid can be readily converted to the corresponding monoalkyl terephthalate in high yield, via a two-step procedure. This method is advantageously compared to the more representative methods described in the literature. The purification of the expected monoester, a crucial problem for this synthetic pathway, is discussed, and an original procedure has been developed. Copyright Taylor & Francis Group, LLC.
Unsymmetrical dicarboxylic esters as bleach precursors
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, (2008/06/13)
A bleach precursor compound, its peroxygen derivative, and detergent compositions containing these materials are disclosed herein. The bleach precursors structurally comprise a pair of different diesters, one ester containing an electrically-charged functional group. Perhydrolysis of the precursor in the presence of hydrogen peroxide and a basic aqueous media generates a peroxycarboxylic acid.