HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035285Generated: October 26, 2026
Toluene → 4,4'-Bis(4-methylbenzyl)-1,1'-biphenyl
https://huagongshe.com/reaction/2035285
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | 4,4'-Bis(chloromethyl)-1,1'-biphenyl | HCID 74275 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,4'-Bis(4-methylbenzyl)-1,1'-biphenyl | HCID 20590984 | — |
Reaction Steps
A 500 mL flask was charged with 4,4′-bis(chloromethyl)-1,1′-biphenyl (25.1 g) and toluene (300 mL). To the clear solution stirring at room temperature was added titanium tetrachloride (1 mL) and the mixture instantly became dark brown. After 5 minutes, a second 1 mL aliquot of catalyst was added. After stirring overnight at room temperature, ethanol (10 mL) was added to kill the catalyst, and the mixture became a light, cream colored suspension. The organic layer was concentrated to dryness under vacuum on a rotary evaporator. The tan solid was suspended in 200 mL boiling toluene and treated with MgSO4. Vacuum filtration through glass fiber filter paper gave a clear solution to which 200 mL heptane was added while hot. The slightly turbid solution was cooled to room temperature, then in a freezer overnight to complete crystallization. White crystals, 17.4 g, mp=161.8 C, were recovered. 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-142a94cea641463989cee6fa590fd6a8 |
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| Source note | uspto-grants-2013_11 |
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