MX3016E - IMPROVED PROCEDURE FOR OBTAINING ETHYLENE GLYCOL ESTERS AND TEREPHTHALIC ACID - Google Patents

IMPROVED PROCEDURE FOR OBTAINING ETHYLENE GLYCOL ESTERS AND TEREPHTHALIC ACID

Info

Publication number
MX3016E
MX3016E MX100139U MX10013975U MX3016E MX 3016 E MX3016 E MX 3016E MX 100139 U MX100139 U MX 100139U MX 10013975 U MX10013975 U MX 10013975U MX 3016 E MX3016 E MX 3016E
Authority
MX
Mexico
Prior art keywords
terephthalic acid
ethylene glycol
glycol
temperature
glycol esters
Prior art date
Application number
MX100139U
Other languages
Spanish (es)
Inventor
Burkhardt Rudolf
Renckhoff Gustav
Schmidt Reinhard
Original Assignee
Dynamit Nobel Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dynamit Nobel Ag filed Critical Dynamit Nobel Ag
Publication of MX3016E publication Critical patent/MX3016E/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/34Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/03Preparation of carboxylic acid esters by reacting an ester group with a hydroxy group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/76Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
    • C07C69/80Phthalic acid esters
    • C07C69/82Terephthalic acid esters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

La presente invención se refiere a un procedimiento mejorado para la obtención de ésteres de etilenglicol y ácido tereftálico, que consiste en la transesterificación contínua de dimetiltereftalato con el glicol del etileno, en una relación molar de: 1.6 a 1 : 2 a temperatura de 140 a 240°C, en un reactor de varias etapas y disminución subsiguiente de la porción de glicol a presión reducida, caracterizado porque se aspira la mezcla de transeterificación a partir de la última etapa del reactor continuamente en una zona de presión reducida, en la cual se mantiene una temperatura de que se halla en 10 a 40°C por encima del punto de solidificación del producto terminal y en donde se regula la presión de tal manera que dentro del tiempo de permanencia en esta zona se separará por destilación del producto una cantidad de glicol necesaria para ajustar la relación molar de ácido tereftálico respecto al glicol en el valor deseado dentro del producto terminal entre 1 : 1.45 y 1 : 1.15, y porque se aplica o se gotea el producto retirado de esta zona sobre una superficie calentada a una temperatura comprendida entre 40°C y 100°C y preferiblemente 70 a 90°C y se separa la misma en forma de escamas sólidas o pastillas.The present invention relates to an improved process for obtaining ethylene glycol and terephthalic acid esters, which consists of the continuous transesterification of dimethylterephthalate with ethylene glycol, in a molar ratio of: 1.6 to 1: 2 at a temperature of 140 to 240 ° C, in a multi-stage reactor and subsequent decrease of the glycol portion at reduced pressure, characterized in that the transeterification mixture from the last stage of the reactor is sucked continuously in a zone of reduced pressure, in which maintains a temperature that is 10 to 40 ° C above the solidification point of the terminal product and where the pressure is regulated in such a way that within the residence time in this area a quantity of glycol required to adjust the molar ratio of terephthalic acid to glycol to the desired value within the end product between 1: 1.45 and 1: 1.15, and because the product removed from this zone is applied or drips onto a surface heated to a temperature between 40 ° C and 100 ° C and preferably 70 to 90 ° C and it separates in the form of solid flakes or tablets.

MX100139U 1975-02-01 1975-11-24 IMPROVED PROCEDURE FOR OBTAINING ETHYLENE GLYCOL ESTERS AND TEREPHTHALIC ACID MX3016E (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19752504156 DE2504156A1 (en) 1975-02-01 1975-02-01 LOW MOLECULAR MOLECULAR TEREPHTHAL ACID AETHYLENE GLYCOLESTER, THEIR PREPARATION AND USE

Publications (1)

Publication Number Publication Date
MX3016E true MX3016E (en) 1980-02-04

Family

ID=5937840

Family Applications (1)

Application Number Title Priority Date Filing Date
MX100139U MX3016E (en) 1975-02-01 1975-11-24 IMPROVED PROCEDURE FOR OBTAINING ETHYLENE GLYCOL ESTERS AND TEREPHTHALIC ACID

Country Status (16)

Country Link
JP (1) JPS51101946A (en)
BE (1) BE838080A (en)
BR (1) BR7600251A (en)
CA (1) CA1081245A (en)
DD (1) DD123738A5 (en)
DE (1) DE2504156A1 (en)
FR (1) FR2299310A1 (en)
GB (1) GB1511412A (en)
IN (1) IN145144B (en)
IT (1) IT1053475B (en)
MX (1) MX3016E (en)
NL (1) NL7600984A (en)
PL (1) PL103014B1 (en)
RO (1) RO69845A (en)
SU (1) SU625598A3 (en)
TR (1) TR18730A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2175897B (en) * 1984-08-14 1987-12-16 Mitsubishi Chem Ind Process for preparing tetramethyl biphenyltetracarboxylate
KR100701842B1 (en) * 1999-08-04 2007-04-02 가부시키가이샤 아이에스 Bis-?-hydroxyethyl terephthalate production process and purification process
US6380352B1 (en) * 2000-08-29 2002-04-30 Eastman Chemical Company Polyester precursor purification process

Also Published As

Publication number Publication date
SU625598A3 (en) 1978-09-25
FR2299310A1 (en) 1976-08-27
JPS51101946A (en) 1976-09-08
GB1511412A (en) 1978-05-17
RO69845A (en) 1981-07-30
FR2299310B1 (en) 1979-05-18
BE838080A (en) 1976-05-14
PL103014B1 (en) 1979-05-31
DD123738A5 (en) 1977-01-12
IN145144B (en) 1978-09-02
IT1053475B (en) 1981-08-31
DE2504156A1 (en) 1976-08-05
NL7600984A (en) 1976-08-03
CA1081245A (en) 1980-07-08
BR7600251A (en) 1976-08-31
TR18730A (en) 1977-07-27

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