Реакция #474156
ord-4d6c9881c1434e48a9e9a4214ee3fcc1
Уравнение реакции
Cyclohexane-1,2-dione
2,6-diisopropylaniline
formic acid
→
title compound
Выход 51.8%
(E)-N-(2-(2,6-diisopropylphenylamino)cyclohex-2-enylidene)-2,6-diisopropylaniline
Выход 51.8%
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1ДругоеSynthesis
- 2ДругоеPrecipitated white crystalline solid
- 3Другоеis collected on the frit
- 4Промывкаwashed with methanol (2×15 mL)
- 5Другоеdried under reduced pressure
- 6Другоеto give
Методика
Synthesis based on literature procedure (Gates, D. P.; Svejda, S. A. Onate, E.; Killian, C. M.; Johnson, L. K.; White, P. S.; Brookhart M. Macromolecules, 2000; 33:2320-2334.). Cyclohexane-1,2-dione (2.062 g, 18.39 mmol) and 2,6-diisopropylaniline (6.52 g, 36.78 mmol) are dissolved in 70 mL of methanol. To this solution is added 1 mL of formic acid and the mixture is stirred for 3 days at room temperature. Precipitated white crystalline solid is collected on the frit, washed with methanol (2×15 mL) and dried under reduced pressure to give 4.1 g (51.8% yield) of title compound of Preparation 1.