Реакция #1668
ord-506fcc7b31c241b1b92a78d6c6e2a5ef
Уравнение реакции
Реагенты
Нет
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Температураthe resulting suspension was refluxed overnight
- 2ДругоеDuring this time a yellow solid was formed
- 3ФильтрацияThe resulting yellow orange solid was filtered off
- 4Промывкаwashed several times with water
- 5Другоеdried
Методика
To solution of sodium methoxide (7.52 g) in methanol (130 ml) was added cyanoacetamide (5.84 g) followed by 2-(4-chlorophenyl)-3-dimethylaminopropenal and the resulting suspension was refluxed overnight. During this time a yellow solid was formed. The mixture was cooled to room temperature and glacial acetic acid (50 ml) was added followed by water (100 ml). The resulting yellow orange solid was filtered off, washed several times with water and dried to yield 8.1 g of 3-cyano-5-(4-chlorophenyl)-2-pyridinone.