HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035284Generated: October 25, 2026
P-Xylene → 4,4'-Bis(2,5-dimethylbenzyl)-1,1'-biphenyl
https://huagongshe.com/reaction/2035284
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Xylene | HCID 7809 | — |
| Reactant | 4,4'-Bis(chloromethyl)-1,1'-biphenyl | HCID 74275 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,4'-Bis(2,5-dimethylbenzyl)-1,1'-biphenyl | HCID 58526741 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08574323B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-b6cc3255943c4ee2ab27ee67d0f892cc |
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| Source note | uspto-grants-2013_11 |
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