Reacción #2890
ord-b9c8478b753b4132a133ace38f7e208b
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otrothe organic layer separated
- 2ExtracciónThe aqueous layer was extracted with dichloromethane
- 3LavadoThe combined organic layers were washed
- 4Otrodried
- 5Otroevaporated
- 6OtroThe residue was purified by flash chromatography
Procedimiento
4-Methyl-5-oxazolecarbonyl chloride (15 g) and N,O-dimethylhydroxylamine hydrochloride (11 g) in dry chloroform (100 ml) were cooled to 0° C. and dry pyridine (28.5 g) was added. The mixture was allowed to warm to room temperature. After 30 minutes aqueous sodium hydrogen carbonate was added and the organic layer separated. The aqueous layer was extracted with dichloromethane. The combined organic layers were washed, dried and evaporated. The residue was purified by flash chromatography to yield the title compound as a white solid. M.p. 59°-60° C.