Reacción #41696
ord-76d5f9db0bc242af8f1bbe578660f790
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otrothe reaction liquid
- 2OtroPyridine was evaporated away under reduced pressure, and water
- 3workup.ADDITIONwas added to it
- 4FiltraciónThe resulting deposit was taken out through filtration
- 5Lavadowashed with water
- 6Otrodried
Procedimiento
5.79 g of N-methoxy-N-methylamine hydrochloride and 12.4 g of 1-ethyl-3-(3′-dimethylaminopropyl)-carbodiimide hydrochloride were added to a pyridine (80 ml) suspension of 10 g of 2-fluoro-4-nitrobenzoic acid, and the reaction liquid was stirred overnight at room temperature. Pyridine was evaporated away under reduced pressure, and water was added to it. The resulting deposit was taken out through filtration, washed with water, and dried to obtain the entitled compound as a pale yellow solid.