Реакция #502061
ord-24b26e57378e449b932dc84b3a06d04a
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ДругоеTo a 200-mL three-necked flask fitted with a stirrer bar
- 2Другоеthe resulted mixture was reacted at 0° C. for 40 minutes
- 3Температураto warm to room temperature
- 4Другоеwas further reacted for another 5 hours
- 5workup.ADDITIONthe reaction solution was poured into a 300-mL separatory funnel
- 6Промывкаwashed with 100 mL of water
- 7Сушкаdried with anhydrous sodium sulfate
- 8ДругоеFrom the obtained solution, the solvent was removed by an evaporator
- 9Другоеto obtain an oily crude product
- 10ДругоеThe crude product was purified by silica gel chromatography
Методика
To a 200-mL three-necked flask fitted with a stirrer bar coated with Teflon™, were added 5.37 g of 4-hydroxytetrahydrothiopyran (manufactured by SANKYO KASEI Co., Ltd.), 5.08 g of triethyl amine, and 50 mL of dried methylene chloride, and the mixture was stirred under nitrogen atmosphere at 0° C. To the mixture, 5.0 g of methacryloyl chloride was slowly added through a dropping funnel, and the resulted mixture was reacted at 0° C. for 40 minutes, allowed to warm to room temperature, and was further reacted for another 5 hours. After confirming loss of the starting material by a thin layer chromatography (TLC), the reaction solution was poured into a 300-mL separatory funnel, washed with 100 mL of water followed by 100 mL of saturated NaCl solution (brine), and dried with anhydrous sodium sulfate. From the obtained solution, the solvent was removed by an evaporator, to obtain an oily crude product. The crude product was purified by silica gel chromatography using a mixed solution of n-hexane and ethyl acetate to give 5.18 g of tetrahydro-2H-thiopyran-4-yl methacrylate (thiopyran derivative of the following formula 2) (yield: 61.3%).