Réaction #50494
ord-b9abcddd57be425a9b079fbae3721260
Équation de réaction
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Températurewas refluxed for 5 hours
- 2AutreAfter the reaction
- 3Autremost of the acetonitrile was removed by distillation and water
- 4workup.ADDITIONwas added to the residue
- 5AutreAs the solid product was separated
- 6Filtrationit was collected by filtration
- 7AutreThe crude material was recrystallized from ethanol
Mode opératoire
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.