反応 #502061

ord-24b26e57378e449b932dc84b3a06d04a

反応方程式

OC1CCSCC1
4-hydroxytetrahydrothiopyran
CCN(CC)CC
triethyl amine
C=C(C)C(=O)Cl
methacryloyl chloride
C=C(C)C(=O)OC1CCSCC1
tetrahydro-2H-thiopyran-4-yl methacrylate
収率 61.3%

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他To a 200-mL three-necked flask fitted with a stirrer bar
  2. 2
    その他the resulted mixture was reacted at 0° C. for 40 minutes
  3. 3
    温度to warm to room temperature
  4. 4
    その他was further reacted for another 5 hours
  5. 5
    workup.ADDITIONthe reaction solution was poured into a 300-mL separatory funnel
  6. 6
    洗浄washed with 100 mL of water
  7. 7
    乾燥dried with anhydrous sodium sulfate
  8. 8
    その他From the obtained solution, the solvent was removed by an evaporator
  9. 9
    その他to obtain an oily crude product
  10. 10
    その他The crude product was purified by silica gel chromatography

実験手順

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%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08088556B2uspto-grants-2012_01