反应 #502061
ord-24b26e57378e449b932dc84b3a06d04a
反应方程式
反应条件
后处理
- 1其他To a 200-mL three-necked flask fitted with a stirrer bar
- 2其他the resulted mixture was reacted at 0° C. for 40 minutes
- 3温度to warm to room temperature
- 4其他was further reacted for another 5 hours
- 5workup.ADDITIONthe reaction solution was poured into a 300-mL separatory funnel
- 6洗涤washed with 100 mL of water
- 7干燥dried with anhydrous sodium sulfate
- 8其他From the obtained solution, the solvent was removed by an evaporator
- 9其他to obtain an oily crude product
- 10其他The crude product was purified by silica gel chromatography
实验过程
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%).