関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Phenol | HCID 996 | — |
| 反応物 | 1,4-Diacetylbenzene | HCID 13888 | — |
| 生成物 | alpha,alpha'-Dimethyl-alpha,alpha,alpha',alpha'-tetrakis(4-hydroxyphenyl)-p-xylene | HCID 22352143 | — |
反応手順
0.0215 mols of α,α′-dimethyl-α,α,α′,α′-tetrakis(4-hydroxyphenyl)-p-xylene (produced from 1,4-diacetylbenzene and phenol and having a melting point of 307° C.), 9.2 mols of bisphenol A, 9.4 liters of an aqueous solution of 2.0 N sodium hydroxide, and 8 liters of dichloromethane were put into a 50 liters container equipped with a stirrer, and stirred therein, to which phosgene was introduced for 30 minutes. Next, 0.44 mols of bisphenol A, 0.022mols of triethylamine, and 4.5 liters of an aqueous solution of 0.2 N sodium hydroxide were added thereto, and reacted for 40 minutes, and thereafter the aqueous phase and the organic phase in the reaction mixture were separated from each other. Thus was prepared a dichloromethane solution of an oligocarbonate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06222004B1 |
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| 出典データセット | uspto-grants-2001_04 |
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| ORD ID | ord-af0f685bc8e84499939123ce07ee12b0 |
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| 出典メモ | uspto-grants-2001_04 |
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