Reacción #550468
ord-70e12156022748f9888e2daa73619856
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Extracciónextracted with ethyl acetate (3×75 ml)
- 2Secadothe combined extracts dried (MgSO4)
- 3Otroevaporated
- 4workup.DISSOLUTIONThe resulting oil (1.3 g) was dissolved in ether
- 5workup.ADDITIONtreated with ethereal hydrogen chloride until precipitation
- 6FiltraciónThe product was filtered off
- 7Otrodried immediately in vacuo
Procedimiento
A solution of 1-[4-(4-chlorophenyl)-2-(4-acetylamino-2,6-dichlorophenoxy)-n-butyl]imidazole (1.58 g) (prepared as in Example 1) in 15 ml of concentrated hydrochloric acid was heated at 90° C. for 1 day. The resulting solution was poured into 200 ml of aqueous potassium carbonate solution, extracted with ethyl acetate (3×75 ml) and the combined extracts dried (MgSO4) and evaporated. The resulting oil (1.3 g) was dissolved in ether and treated with ethereal hydrogen chloride until precipitation was complete. The product was filtered off and dried immediately in vacuo to give 1.4 g of 1-[4-(4-chlorophenyl)-2-(4-amino-2,6-dichlorophenoxy)-n-butyl]imidazole bis(hydrochloride), m.p. 119°-123° C.