Реакция #2122467
ord-142a94cea641463989cee6fa590fd6a8
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.ADDITIONa second 1 mL aliquot of catalyst was added
- 2workup.STIRRINGAfter stirring overnight at room temperature
- 3КонцентрированиеThe organic layer was concentrated to dryness under vacuum on a rotary evaporator
- 4workup.ADDITIONtreated with MgSO4
- 5ФильтрацияVacuum filtration through glass fiber
- 6Фильтрацияfilter paper
- 7Другоеgave a clear solution to which 200 mL heptane
- 8workup.ADDITIONwas added while hot
- 9ТемператураThe slightly turbid solution was cooled to room temperature
- 10workup.WAITin a freezer overnight to complete
- 11Другоеcrystallization
- 12ДругоеWhite crystals, 17.4 g, mp=161.8 C, were recovered
Методика
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.