Реакция #2486959
ord-b2b0129939c94941b5b2903cac702def
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1Другоеat room temperature
- 2workup.STIRRINGwith stirring
- 3workup.WAITthe stirring was continued for 2 hours
- 4ПромывкаThe aqueous layer was further washed with diethyl ether (50 ml)
- 5СушкаThe combined organic layer was dried over magnesium sulfate
- 6Концентрированиеconcentrated under reduced pressure
- 7workup.ADDITIONTo the resulting residue were added water (25 ml) and 37% aqueous formaldehyde (8 ml) at room temperature
- 8workup.STIRRINGby vigorous stirring at room temperature
- 9workup.ADDITIONAfter addition of an aqueous solution (36 ml) of potassium carbonate (6.5 g) over 5 minutes
- 10Другоеthe mixture reaction
- 11workup.STIRRINGwas stirred for 4 hours
- 12Экстракцияextracted with diethyl ether (100 ml×2)
- 13СушкаThe extract was dried over anhydrous magnesium sulfate
- 14Концентрированиеconcentrated under reduced pressure
Методика
Metal sodium (1.5 g) was gradually added to ethanol (50 ml) at room temperature, followed by stirring for 5 minutes, and diethyl carbonate (8.9 ml, 73 mmol) was added thereto at room temperature. Further, a solution of ethyl 4-chlorophenylacetate (10 g) in ethanol (10 ml) was added dropwise thereto with stirring, and the stirring was continued for 2 hours. The reaction mixture was concentreated, and diethyl ether (150 ml) and 10% aqueous acetic acid (150 ml) were added to the residue for extraction. The aqueous layer was further washed with diethyl ether (50 ml). The combined organic layer was dried over magnesium sulfate and concentrated under reduced pressure. To the resulting residue were added water (25 ml) and 37% aqueous formaldehyde (8 ml) at room temperature, followed by vigorous stirring at room temperature. After addition of an aqueous solution (36 ml) of potassium carbonate (6.5 g) over 5 minutes, the mixture reaction was stirred for 4 hours and extracted with diethyl ether (100 ml×2). The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give a crude product of ethyl 4-chlorophenyl-α-methyleneacetate (yield, 10 g).