참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrachloro-p-hydroquinone | HCID 66603 | — |
| 반응물 | Tetrafluorophthalonitrile | HCID 74600 | — |
| 생성물 | 1,4-Bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene | HCID 11330937 | — |
반응 단계
The objective 1,4-bis(3,4-dicarboxytrifluorophenoxy)tetrachlorobenzene dianhydride is produced as an embodiment by reacting tetrafluorophthalonitrile and tetrachlorohydroquinone (or its metal salts such as 2 Na salt; it is summarized as “tetrachlorohydroquinone”) in the presence of a base in a solvent at a temperature of −20° C. to 200° C. for 0.1 to 20 hours to form 1,4-bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene (Step 1a); hydrolyzing the resulting 1,4-bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene with an acid at a temperature of 50° C. to 300° C. for 0.5 to 20 hours to form 1,4-bis(3,4-dicarboxytrifluorophenoxy)tetrachlorobenzene (Step 1b); dissolving the reaction solution including 1,4-bis(3,4-dicarboxytrifluorophenoxy)tetrachlorobenzene in a medium containing an organic solvent once, purifying and separating the product therefrom (Step 1c); and then dehydrating the separated 1,4-bis(3,4-dicarboxytrifluorophenoxy)tetrachlorobenzene (Step 1d).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06916959B2 |
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| 출처 데이터셋 | uspto-grants-2005_07 |
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| ORD ID | ord-7011c87327d6418db94653766a998e8b |
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| 출처 메모 | uspto-grants-2005_07 |
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