Реакция #463374
ord-5bf4fd617c3947b79db07548dfc8823c
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1ТемператураThen, the temperature was raised to -25° C
- 2workup.STIRRINGunder stirring
- 3Температураwhile maintaining the temperature at -25° C
- 4workup.ADDITIONAfter the dropwise addition
- 5Температураthe temperature was raised to room temperature
- 6workup.STIRRINGwith stirring
- 7Температураunder cooling with ice
- 8ТемператураThen, the temperature was raised to room temperature
- 9Другоеfor liquid separation
- 10ДругоеThe organic layer was collected by separation
- 11workup.ADDITIONpost-treated by a conventional method
- 12ДругоеThe product was purified by silica gel column chromatography (hexane/ethyl acetate=4/1)
Методика
9.45 g of methyl (R)-(-)-3-hydroxybutyrate was dissolved in 200 ml of tetrahydrofuran, and 112 ml of a 1.5M cyclohexane solution of lithium diisopropylamide was added thereto with stirring under cooling to -70° C. Then, the temperature was raised to -25° C. Then, 35 ml of a hexamethylphosphoric triamide solution of 21.1 g of 3,4-dichlorobenzyl bromide was dropwise added to this solution under stirring while maintaining the temperature at -25° C. After the dropwise addition, the temperature was raised to room temperature. Then, a saturated ammonium chloride aqueous solution was added to the reaction solution with stirring under cooling with ice. Then, the temperature was raised to room temperature, and ethyl ether and water were added thereto for liquid separation. The organic layer was collected by separation and post-treated by a conventional method. The product was purified by silica gel column chromatography (hexane/ethyl acetate=4/1) to obtain 10.6 g (yield: 48%) of methyl (2R, 3R)-2-(3,4-dichlorobenzyl)-3-hydroxybutyrate.