Reacción #502062

ord-05b04d24f6524d55b68b5143f3daa0d9

Ecuación de reacción

CC1(O)CCSCC1
4-hydroxy-4-methyltetrahydrothiopyran
CCN(CC)CC
triethyl amine
C=C(C)C(=O)Cl
methacryloyl chloride
C=C(C)C(=O)OC1(C)CCSCC1
4-methyl-tetrahydro-2H-thiopyran-4-yl methacrylate
Rendimiento 65.3%

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroTo a 200-mL three-necked flask fitted with a stirrer bar
  2. 2
    Otrothe resulted mixture was reacted at 0° C. for 30 minutes
  3. 3
    Temperaturato warm to room temperature
  4. 4
    Otrowas further reacted for another 5 hours
  5. 5
    workup.ADDITIONthe reaction solution was poured in a 300-mL separatory funnel
  6. 6
    Lavadowashed with 100 mL of water
  7. 7
    Secadodried with anhydrous sodium sulfate
  8. 8
    OtroFrom the obtained solution, the solvent was removed by an evaporator
  9. 9
    Otroto obtain an oily crude product
  10. 10
    OtroThe 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%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08088556B2uspto-grants-2012_01