GB984150A - Process for the manufacture of linear copolyesters - Google Patents

Process for the manufacture of linear copolyesters

Info

Publication number
GB984150A
GB984150A GB2342361A GB2342361A GB984150A GB 984150 A GB984150 A GB 984150A GB 2342361 A GB2342361 A GB 2342361A GB 2342361 A GB2342361 A GB 2342361A GB 984150 A GB984150 A GB 984150A
Authority
GB
United Kingdom
Prior art keywords
heptane
spiro
dicarboxylic acid
dimethylol
dihydric alcohol
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
GB2342361A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst 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 Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB984150A publication Critical patent/GB984150A/en
Expired legal-status Critical Current

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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/16Dicarboxylic acids and dihydroxy compounds
    • C08G63/18Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
    • C08G63/199Acids or hydroxy compounds containing cycloaliphatic rings
    • 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
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/06Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

3,6-Dimethylol spiro [3.3] heptane is made by dissolving 3.6-dicarbomethoxy spiro [3.3] heptane in ether and reducing it with lithium aluminium hydride.ALSO:Linear copolyesters containing spiro-[3,3]-heptane rings and suitable for the manufacture of readily dyeable fibres and films are made by reacting (a) spiro-[3,3]-heptane-3,6-dicarboxylic acid, another dicarboxylic acid and a dihydric alcohol, or (b) 3,6-dimethylol spiro-[3,3]-heptane, another dihydric alcohol and a dicarboxylic acid, or (c) spiro-[3,3]-heptane-3,6-dicarboxylic acid, another dicarboxylic acid, 3,6-dimethylol spiro-[3,3]-heptane and another dihydric alcohol. Suitable other acids are adipic, sebacic, 4,41-diphenyldicarboxylic, 2,5-thiophenedicarboxylic, or pyridine-2,5-dicarboxylic acid or acids of formula <FORM:0984150/C3/1> where R is a bivalent radical, e.g. -CH2-, -CH2-CH2-, -CH = CH- -CH2OCH2-or -SO2-. The other dihydric alcohol may be ethylene-, trimethylene-, tetramethylene-, neopentyl-, diethylene- or p-xylylene glycol or 1,4-dimethylol cyclohexane. Ester-forming derivatives of the acids and/or alcohol may be used. In examples, copolyesters are made by reacting (1) spiro-[3,3]-heptane-3,6-dicarboxylic acid dimethyl ester, dimethyl terephthalate and ethylene glycol; (2) spiro-[3,3]-heptane-3,6-dicarboxylic acid dimethyl ester and ethylene glycol followed by the addition of bis-(b -hydroxyethyl) terephthalate and further reaction; (3) spiro-[3,3]-heptane-3,6-dimethylol and dimethyl terephthalate, followed by the addition of bis-(b -hydroxyethyl) terephthalate and further reaction.
GB2342361A 1960-07-02 1961-06-28 Process for the manufacture of linear copolyesters Expired GB984150A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF0031570 1960-07-02

Publications (1)

Publication Number Publication Date
GB984150A true GB984150A (en) 1965-02-24

Family

ID=7094253

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2342361A Expired GB984150A (en) 1960-07-02 1961-06-28 Process for the manufacture of linear copolyesters

Country Status (3)

Country Link
BE (1) BE605669A (en)
GB (1) GB984150A (en)
NL (1) NL266404A (en)

Also Published As

Publication number Publication date
BE605669A (en) 1962-01-03
NL266404A (en)

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