Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Dimethyl 1,4-cyclohexanedicarboxylate | HCID 7198 | — |
| Reactant | Dimethyl terephthalate | HCID 8441 | — |
| Reactant | Oxo(oxostibanyloxy)stibane | HCID 27652 | — |
| Catalyst | Zinc acetate (USP) | HCID 2724192 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86739121 | HCID 86739121 | — |
Reaction Steps
A mixture of dimethyl 1,4-cyclohexanedicarboxylate (88.1 g, 0.40 mole), dimethyl terephthalate (194.0 g, 1.0 mole), and ethylene glycol (147.7 g, 1.7 mole) in the presence of zinc diacetate dihydrate (0.0629 g) and antimony trioxide (0.158 g) was heated at 200° C. under a slow stream of nitrogen overnight until the evolution of methanol ceased. The temperature was increased to 240° C., and the mixture was stirred under reduced pressure (0.025 mm Hg) for 3 hours until the stirring was difficult. The reaction mixture on cooling under nitrogen afforded a water white, amorphous polymer Tg 59° C., I.V. 0.58 dl/g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04416965 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-8a0ff486f2314db08772ef494525070f |
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| Source note | uspto-grants-1983_11 |
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