HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2035284Erstellt: 26. Oktober 2026
P-Xylene → 4,4'-Bis(2,5-dimethylbenzyl)-1,1'-biphenyl
https://huagongshe.com/reaction/2035284
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | P-Xylene | HCID 7809 | — |
| Edukt | 4,4'-Bis(chloromethyl)-1,1'-biphenyl | HCID 74275 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4,4'-Bis(2,5-dimethylbenzyl)-1,1'-biphenyl | HCID 58526741 | — |
Reaktionsschritte
A 100mL flask was charged with 4,4′-bis(chloromethyl)-1,1′-biphenyl (1.0 g) and p-xylene (25 mL). To the clear solution stirring at room temperature was added titanium tetrachloride (6 drops) and the mixture instantly became dark brown. After stirring overnight at room temperature, ethanol (2mL) was added to kill the catalyst, and the mixture became a light, cream colored suspension. The mixture was transferred to a separatory funnel and washed with dilute aqueous HCl followed by saturated aqueous sodium bicarbonate. The organic layer was dried over magnesium sulfate, and concentrated to dryness under vacuum on a rotary evaporator. The tan solid was recrystallized from toluene yielding a white crystalline product, mp=144.6 C. GC/MS, HNMR, CNMR and IR were all consistent with the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08574323B2 |
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| Quelldatensatz | uspto-grants-2013_11 |
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| ORD ID | ord-b6cc3255943c4ee2ab27ee67d0f892cc |
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| Quellennotiz | uspto-grants-2013_11 |
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