Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bischlorophthalimide | HCID 14948820 | — |
| Reactant | disodium bisphenol-A | HCID 66941220 | — |
| Reactant | 4,4'-Biphenol disodium salt | HCID 67055508 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | Bisphenol A | HCID 6623 | — |
Reaction Steps
Bisphenol A disodium salt (4.6981 g, 17.2562 mmol), 4,4′-biphenol disodium salt (2.6479 g, 11.5042 mmol), and o-DCB (60 mL) were combined in a reaction vessel equipped with a mechanical stirrer, short path distillation head, receiver, and inert gas inlet and exit. o-DCB was distilled from the mixture until the distillate contained less than 10 ppm of water. Approximately 20 to 30 mL of o-DCB was removed in this drying step. Then, 15.3885 g (29.0716 mmol) of the bischlorophthalimide prepared from ODA and 98% 3ClPA, 2% 4ClPA, and 0.1334 g (0.5177 mmol) of 4-chloro-N-methyl phthalimide chain stopper were added quantitatively to the reaction vessel along with 10-20 mL of additional o-DCB. O-DCB was distilled from the mixture until a solids level of 25% was reached. Hexaethylguanidium chloride phase transfer catalyst (0.7 mole %) was then added and polymerization initiated. The product polyetherimide had a weight average molecular weight (Mw) of 60,282 grams per mole and a number average molecular weight (Mn) of 24,100 grams per mole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605222B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-1d77988153b84e52b1ee3e92e70195d9 |
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| Source note | uspto-grants-2009_10 |
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