HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 895834Erstellt: 24. Oktober 2026
Tetrachloro-p-hydroquinone → 1,4-Bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene
https://huagongshe.com/de/reaction/895834
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Tetrachloro-p-hydroquinone | HCID 66603 | — |
| Edukt | Tetrafluorophthalonitrile | HCID 74600 | — |
| Produkt | 1,4-Bis(3,4-dicyanotrifluorophenoxy)tetrachlorobenzene | HCID 11330937 | — |
Reaktionsschritte
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).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06916959B2 |
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| Quelldatensatz | uspto-grants-2005_07 |
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| ORD ID | ord-7011c87327d6418db94653766a998e8b |
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| Quellennotiz | uspto-grants-2005_07 |
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