Реакция #2066
ord-513ee407692540e49f626f2d20b712d3
Уравнение реакции
Реагенты
Условия реакции
Обработка
- 1Другоеwas 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
- 4Температураthe reaction mixture was warmed to 0° C.
- 5workup.STIRRINGstirred for one hour
- 6ДругоеThe reaction was quenched
- 7workup.ADDITIONby pouring slowly into a well-stirred ice-cold mixture of ethanol (40 ml) and concentrated HCl (5 ml)
- 8ДругоеThe solvents were removed in vacuo
- 9Экстракцияextracted with dichloromethane (4×20 ml)
- 10СушкаThe combined extracts were dried (Na2SO4)
- 11Концентрированиеconcentrated in vacuo
- 12Другоеthe resulting oil was purified by flash chromatography on silica gel eluting with 10% i-propanol in ethyl acetate
Методика
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.