Реакция #1435701
ord-dd590dc6069b484bbd50972ff09490a8
Уравнение реакции
piperidine
2-(2-tert-butyl-6-methyl-pyran-4-ylidene)-malononitrile
5-(4-diphenylamino-phenyl)-thiophene-2-carbaldehyde
→
target compound
Выход 50.0%
2-(2-tert-butyl-6-{2-[5-(4-diphenylamino-phenyl)-thiophene-2-yl]-vinyl}-pyran-4-ylidene)-malononitrile
Выход 50.0%
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1workup.ADDITIONwas added
- 2ТемператураThe reaction solution was heated for 24 hours
- 3Температураwhile refluxing
- 4ТемператураAfter cooling the reaction solution
- 5Фильтрацияthe precipitated red solid was filtered
- 6Другоеrecrystallized 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%).