Réaction #2122466

ord-b6cc3255943c4ee2ab27ee67d0f892cc

Équation de réaction

ClCc1ccc(-c2ccc(CCl)cc2)cc1
4,4′-bis(chloromethyl)-1,1′-biphenyl
Cc1ccc(C)cc1
p-xylene
Cc1ccc(C)c(Cc2ccc(-c3ccc(Cc4cc(C)ccc4C)cc3)cc2)c1
4,4′-bis(2,5-dimethylbenzyl)-1,1′-biphenyl

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGAfter stirring overnight at room temperature
  2. 2
    AutreThe mixture was transferred to a separatory funnel
  3. 3
    Lavagewashed with dilute aqueous HCl
  4. 4
    SéchageThe organic layer was dried over magnesium sulfate
  5. 5
    Concentrationconcentrated to dryness under vacuum on a rotary evaporator
  6. 6
    AutreThe tan solid was recrystallized from toluene yielding a white crystalline product, mp=144.6 C

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08574323B2uspto-grants-2013_11