Реакция #1435701

ord-dd590dc6069b484bbd50972ff09490a8

Уравнение реакции

C1CCNCC1
piperidine
CC1=CC(=C(C#N)C#N)C=C(C(C)(C)C)O1
2-(2-tert-butyl-6-methyl-pyran-4-ylidene)-malononitrile
O=Cc1ccc(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)s1
5-(4-diphenylamino-phenyl)-thiophene-2-carbaldehyde
CC(C)(C)C1=CC(=C(C#N)C#N)C=C(C=Cc2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)O1
target compound
Выход 50.0%
CC(C)(C)C1=CC(=C(C#N)C#N)C=C(C=Cc2ccc(-c3ccc(N(c4ccccc4)c4ccccc4)cc3)s2)O1
2-(2-tert-butyl-6-{2-[5-(4-diphenylamino-phenyl)-thiophene-2-yl]-vinyl}-pyran-4-ylidene)-malononitrile
Выход 50.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added
  2. 2
    ТемператураThe reaction solution was heated for 24 hours
  3. 3
    Температураwhile refluxing
  4. 4
    ТемператураAfter cooling the reaction solution
  5. 5
    Фильтрацияthe precipitated red solid was filtered
  6. 6
    Другоеrecrystallized with ethanol

Методика

As shown in the following reaction 3, 0.72 g (3.37 mmol) of (2-(2-tert-butyl-6-methyl-pyran-4-ylidene)-malononitrile and 1 g (2.81 mmol) of 5-(4-diphenylamino-phenyl)-thiophene-2-carbaldehyde were added into 50 ml of ethanol, and 0.28 g (3.37 mmol) of piperidine was added thereto. The reaction solution was heated for 24 hours while refluxing. After cooling the reaction solution, the precipitated red solid was filtered, and recrystallized with ethanol to obtain 0.79 g of the target compound (Yield 50%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07211335B2uspto-grants-2007_05