Реакция #493549
ord-a1c3ad42df04461db79b9e1cc1260091
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1workup.ADDITIONAfter completion of the dropwise addition
- 2workup.STIRRINGAfter stirring for five minutes
- 3Другоеthe organic layer was separated
- 4ПромывкаThe combined organic layers were sequentially washed with 1 N hydrochloric acid, water
- 5Сушкаa saturated sodium bicarbonate aqueous solution and brine, dried over anhydrous magnesium sulfate
- 6Концентрированиеconcentrated under reduced pressure
- 7ДругоеThe resulting residue was purified by silica gel column chromatography (carrier: Wakogel C-200; elution solvent:heptane:ethyl acetate=49:1→19:1)
Методика
Methyl dichlorophosphate (1.9 mL) was added dropwise at 20° C. or less to an ice-cooled solution of 5-chloro-2-(4-chloro-2-trifluoromethylphenyl)pentanoic acid amide (3.0 g) and 1,8-diazabicyclo[5,4,0]undec-7-ene (6.4 mL) in methylene chloride (30 mL). After completion of the dropwise addition, the reaction solution was stirred at room temperature for one hour and 25 minutes. A saturated sodium bicarbonate aqueous solution was added to the reaction solution. After stirring for five minutes, the organic layer was separated. The aqueous layer was reextracted with methylene chloride. The combined organic layers were sequentially washed with 1 N hydrochloric acid, water, a saturated sodium bicarbonate aqueous solution and brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (carrier: Wakogel C-200; elution solvent:heptane:ethyl acetate=49:1→19:1) to obtain 2.25 g of the title compound.