HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 513912Erstellt: 26. Oktober 2026
Tetraethylammonium Hydroxide → Bisphenylcarbazole
https://huagongshe.com/reaction/513912
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetraethylammonium Hydroxide | HCID 6509 | — |
| Edukt | 3-Iodophenylcarbazole | HCID 67051408 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | Bisphenylcarbazole | HCID 23509207 | — |
Reaktionsschritte
91 g (242 mmol) of 3-iodophenylcarbazole 11 and 91 g (246 mmol) of phenylcarbazoleboronic ester 12 are suspended in acetone, and a 350 ml of 20% tetraethylammonium hydroxide solution (493 mmol) are added, the mixture is carefully degassed using argon. 4.6 g (4 mmol) of tetrakis-triphenylphosphinepalladium are subsequently added. The reaction is heated to 70° C. The progress of the reaction is followed by means of thin-layer chromatography. When the reaction is complete, the batch is cooled to room temperature, and the precipitated product is filtered off with suction. The crude product is recrystallised from acetonitrile, giving a beige solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09102797B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-3460e18f67e64267b97550c0a5c48f8c |
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| Quellennotiz | uspto-grants-2015_08 |
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