Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetoacetic Acid | HCID 96 | — |
| Edukt | Acetate | HCID 175 | — |
| Edukt | Bisphenol A | HCID 6623 | — |
| Lösungsmittel | Diphenyl Ether | HCID 7583 | — |
| Produkt | Bisphenol A | HCID 6623 | — |
| Produkt | 1,4-Benzenedicarboxylate | HCID 154269 | — |
Reaktionsschritte
In a 0.5 liter flask equipped wiht a stirrer, thermometer, a distillation set-up and an argon inlet tube are placed 15.617 gms (0.05 mole) of the diacetate of bisphenol-A, 0.05 moles of the acetate of the monofunctional polyphenylene oxide prepared in Example 1, possessing a molecular weight of about 5,500 and having the structure: ##STR11## and 6.04 (0.037 moles) of each terephthalic and isophthalic acids. To this mixture are added about 100 ml of diphenyl ether. Heating, stirring and argon circulation are started. When the temperature reaches about 250° C. strong distillation of acetic acid is observed. The reaction mixture is gradually heated to 290° C. with continuous distillation of acetic acid and diphenyl ether. After 5 hrs a very viscous melt is obtained (290° C.). The melt is cooled and finely ground. A quantitative yield of a slightly yellow copolymer of polyphenylene oxide and the poly(iso/terephthalate) (1:1) of bisphenol-A results.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04746709 |
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| Quelldatensatz | uspto-grants-1988_05 |
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| ORD ID | ord-b6c501b27de442a78b2f500dbbf59b0a |
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| Quellennotiz | uspto-grants-1988_05 |
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