Reacción #2066
ord-513ee407692540e49f626f2d20b712d3
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Otrowas consumed (~20 minutes)
- 2workup.ADDITIONethylmagnesium bromide (1.0 ml of a 3.0M solution in diethyl ether, 3.0 mmol) was added
- 3workup.ADDITIONAfter the addition
- 4Temperaturathe reaction mixture was warmed to 0° C.
- 5workup.STIRRINGstirred for one hour
- 6OtroThe reaction was quenched
- 7workup.ADDITIONby pouring slowly into a well-stirred ice-cold mixture of ethanol (40 ml) and concentrated HCl (5 ml)
- 8OtroThe solvents were removed in vacuo
- 9Extracciónextracted with dichloromethane (4×20 ml)
- 10SecadoThe combined extracts were dried (Na2SO4)
- 11Concentraciónconcentrated in vacuo
- 12Otrothe resulting oil was purified by flash chromatography on silica gel eluting with 10% i-propanol in ethyl acetate
Procedimiento
A solution of N-methoxy-N-methyl-3,3-bis(diethoxyphosphinyl)propionamide (1.00 g, 2.6 mmol) in THF (5 ml) was slowly added to a slurry of 80% sodium hydride (80 mg, 2.7 mmol) in THF (10 ml) at 0° C. Stirring was continued until all of the hydride was consumed (~20 minutes). The solution was cooled to -78° C. and ethylmagnesium bromide (1.0 ml of a 3.0M solution in diethyl ether, 3.0 mmol) was added. After the addition, the reaction mixture was warmed to 0° C. and stirred for one hour. The reaction was quenched by pouring slowly into a well-stirred ice-cold mixture of ethanol (40 ml) and concentrated HCl (5 ml). The solvents were removed in vacuo, the residue was taken up in brine (20 ml) and extracted with dichloromethane (4×20 ml). The combined extracts were dried (Na2SO4), concentrated in vacuo, and the resulting oil was purified by flash chromatography on silica gel eluting with 10% i-propanol in ethyl acetate to give the title compound (0.50 g, 54%) as a pale yellow oil.