Реакция #50494
ord-b9abcddd57be425a9b079fbae3721260
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Температураwas refluxed for 5 hours
- 2ДругоеAfter the reaction
- 3Другоеmost of the acetonitrile was removed by distillation and water
- 4workup.ADDITIONwas added to the residue
- 5ДругоеAs the solid product was separated
- 6Фильтрацияit was collected by filtration
- 7ДругоеThe crude material was recrystallized from ethanol
Методика
A mixture of 2.9 g of 2-nitroiminothiazolidine, 2.9 g of anhydrous potassium carbonate, 3.2 g of 2-chloro-5-pyridylmethylchloride and 50 ml of acetonitrile was refluxed for 5 hours with vigorously stirring. After the reaction, most of the acetonitrile was removed by distillation and water was added to the residue. As the solid product was separated, it was collected by filtration. The crude material was recrystallized from ethanol to give desired 3-(2-chloro-5-pyridylmethyl)-2-(nitroimino)thiazolidine.