Реакция #474156

ord-4d6c9881c1434e48a9e9a4214ee3fcc1

Уравнение реакции

O=C1CCCCC1=O
Cyclohexane-1,2-dione
CC(C)c1cccc(C(C)C)c1N
2,6-diisopropylaniline
O=CO
formic acid
CC(C)c1cccc(C(C)C)c1/N=C1\CCCC=C1Nc1c(C(C)C)cccc1C(C)C
title compound
Выход 51.8%
CC(C)c1cccc(C(C)C)c1/N=C1\CCCC=C1Nc1c(C(C)C)cccc1C(C)C
(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

  1. 1
    ДругоеSynthesis
  2. 2
    ДругоеPrecipitated white crystalline solid
  3. 3
    Другоеis collected on the frit
  4. 4
    Промывкаwashed with methanol (2×15 mL)
  5. 5
    Другоеdried under reduced pressure
  6. 6
    Другоеto 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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08372927B2uspto-grants-2013_02