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ChemicalBook CAS DataBase List TEREPHTHALIC ACID 2-HYDROXYETHYL METHYL ESTER

TEREPHTHALIC ACID 2-HYDROXYETHYL METHYL ESTER synthesis

8synthesis methods
-

Yield:-

Reaction Conditions:

1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine for 24 h;Product distribution / selectivity;

Steps:

32
Comparison Examples 29 to 34Glycolysis of Dimethyl Terephthalate (DMT) at Ambient Temperature with DBU and TBDMaterials. DMT and Amberlyst-15 was purchased from Sigma-Aldrich and used as received.To a 5 ml sample tube containing DMT (0.48 g, 2.5 mmol) was charged predetermined amounts of EG and a catalyst (DBU or TBD, 0.125 mmol, 0.05 eq.). Three levels of EG were used with each catalyst: 2.84 molar equivalents, 8 molar equivalents, and 16 molar equivalents of EG relative to moles of DMT. After the mixture was stirred for 24 hours, THF (8 mL) and Amberlyst-15 (150 mg) were added to the mixture to quench the reaction and allow the slurry to become homogeneous. Aliquots of the solution were taken for 1H NMR and GPC analysis in order to evaluate the conversion and content. FIG. 12 shows a typical GPC curve of the crude product. Peak labeled A corresponds to oligomers, peak labeled B corresponds to BHET, peak labeled C corresponds to 2-hydroxyethyl methyl terephthalate (HEMT), and peaks labeled D correspond to EG and DMT. HEMT is the intermediate in glycolysis of DMT and has the following structure:The GPC results are summarized in Table 6 below.

References:

KING ABDULAZIZ CITY FOR SCIENCE AND TECHNOLOGY;INTERNATIONAL BUSINESS MACHINES CORPORATION US2012/223270, 2012, A1 Location in patent:Page/Page column 15

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