SU1363755A1 - Method of tere- or isophthalic acid esters synthesis - Google Patents

Method of tere- or isophthalic acid esters synthesis

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Publication number
SU1363755A1
SU1363755A1 SU4066869/04A SU4066869A SU1363755A1 SU 1363755 A1 SU1363755 A1 SU 1363755A1 SU 4066869/04 A SU4066869/04 A SU 4066869/04A SU 4066869 A SU4066869 A SU 4066869A SU 1363755 A1 SU1363755 A1 SU 1363755A1
Authority
SU
USSR - Soviet Union
Prior art keywords
phenol
bis
tere
carried out
isophthalic acid
Prior art date
Application number
SU4066869/04A
Other languages
Russian (ru)
Inventor
С.А. Радзинский
М.М. Кляцкин
В.В. Америк
В.В. Гурьянова
Т.Н. Прудскова
А.В. Павлов
Original Assignee
Научно-исследовательский институт пластических масс им.Г.С.Петрова Научно-исследовательского объединения "Пластмассы"
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 Научно-исследовательский институт пластических масс им.Г.С.Петрова Научно-исследовательского объединения "Пластмассы" filed Critical Научно-исследовательский институт пластических масс им.Г.С.Петрова Научно-исследовательского объединения "Пластмассы"
Priority to SU4066869/04A priority Critical patent/SU1363755A1/en
Application granted granted Critical
Publication of SU1363755A1 publication Critical patent/SU1363755A1/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

FIELD: organic chemistry, esters of aromatic acids. SUBSTANCE: synthesis is carried out from bis-phenol of the general formula C(CH)(R), where R -;- H, Br and NaOH in water following by condensation with tere- or isophthalic acid chloroanhydride in the medium of organic solvent. Molar ratio of bis-phenol: NaOH: water = = 1: 1: (8,4-12,9). Process is carried out at 75-85 C up to preparing of homogeneous solution. After cooling of latter condensation in suspension of acid chloroanhydrides is carried out. Time of process is shortened by 2-15-times without sewage formation. Conversion of bis-phenol is increased by 3,4-8,2% . EFFECT: intensification of process, enhanced conversion of bis-phenol. 1 tbl
SU4066869/04A 1986-05-13 1986-05-13 Method of tere- or isophthalic acid esters synthesis SU1363755A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU4066869/04A SU1363755A1 (en) 1986-05-13 1986-05-13 Method of tere- or isophthalic acid esters synthesis

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU4066869/04A SU1363755A1 (en) 1986-05-13 1986-05-13 Method of tere- or isophthalic acid esters synthesis

Publications (1)

Publication Number Publication Date
SU1363755A1 true SU1363755A1 (en) 1994-02-15

Family

ID=60519493

Family Applications (1)

Application Number Title Priority Date Filing Date
SU4066869/04A SU1363755A1 (en) 1986-05-13 1986-05-13 Method of tere- or isophthalic acid esters synthesis

Country Status (1)

Country Link
SU (1) SU1363755A1 (en)

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