Reacción #502062
ord-05b04d24f6524d55b68b5143f3daa0d9
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroTo a 200-mL three-necked flask fitted with a stirrer bar
- 2Otrothe resulted mixture was reacted at 0° C. for 30 minutes
- 3Temperaturato warm to room temperature
- 4Otrowas further reacted for another 5 hours
- 5workup.ADDITIONthe reaction solution was poured in a 300-mL separatory funnel
- 6Lavadowashed with 100 mL of water
- 7Secadodried with anhydrous sodium sulfate
- 8OtroFrom the obtained solution, the solvent was removed by an evaporator
- 9Otroto obtain an oily crude product
- 10OtroThe crude product was purified by silica gel chromatography
Procedimiento
To a 200-mL three-necked flask fitted with a stirrer bar coated with Teflon™, were added 5.95 g of 4-hydroxy-4-methyltetrahydrothiopyran (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 30 minutes, allowed to warm to room temperature, and was further reacted for another 5 hours. After confirming loss of the starting material by TLC, the reaction solution was poured in a 300-mL separatory funnel, washed with 100 mL of water followed by with 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 5.89 g of 4-methyl-tetrahydro-2H-thiopyran-4-yl methacrylate (thiopyran derivative of the following formula 3) (yield: 59.4%).