Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bisphenol B | HCID 66166 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Bisphenol E | HCID 608116 | — |
Reaktionsschritte
A methylene chloride solution of a bisphenol B oligomer having a chloroformate group at its molecular terminal was obtained in the same manner as that in Manufacturing Example 1 except that the bisphenol E was replaced by 65.8 g (0.272 mol) of 2,2-bis(4-hydroxyphenyl)butane (BisB), the amount of triethylamine was changed to 53.8 g (0.533 mol), and the methylene chloride solution of phosgene was replaced by a solution in which 52.7 g (0.533 mol) of phosgene was dissolved in 225 mL of methylene chloride in Manufacturing Example 1. The obtained solution had a chloroformate concentration of 0.99 mol/L, a solid concentration of 0.21 kg/L and an average number of repeating units (n′) of 1.21. A content of an amide compound in the obtained BisB oligomer was found to be 90 mass ppm. A mass of nitrogen derived from triethylamine was 0.3 mass ppm. This obtained ingredient will be referred to as “BisB-CF” hereinafter.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08519082B2 |
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| Quelldatensatz | uspto-grants-2013_08 |
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| ORD ID | ord-1a31e22a50134bb2890c7d09fbe1433d |
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| Quellennotiz | uspto-grants-2013_08 |
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