Reacción #2304292

ord-947b6c23bb5f4070815ddde55ec7c33b

Ecuación de reacción

CCOC(=O)CCc1ccc(O)cc1
ethyl 3-(4-hydroxyphenyl)propionate
[K+].[OH-]
potassium hydroxide
CCO
ethanol
CCC1(COS(=O)(=O)c2ccc(C)cc2)COC1
3-[(tosyloxy)methyl]-3-ethyloxetane
CCC1(COc2ccc(C(C)C(=O)O)cc2)COC1
[4-(3-ethyloxetan-3-ylmethoxy)phenyl]propionic acid

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThis was cooled to 40° C.
  2. 2
    TemperaturaThen, this was refluxed for 3 hours
  3. 3
    OtroEthanol was evaporated away
  4. 4
    workup.ADDITIONwater and toluene were added to it for liquid-liquid separation
  5. 5
    LavadoThe toluene layer was washed with 3% hydrochloric acid, saturated sodium hydrogencarbonate and water
  6. 6
    Otrotoluene was evaporated away
  7. 7
    workup.ADDITIONTo the resulting residue, added
  8. 8
    Temperaturathis was refluxed for 2 hours
  9. 9
    OtroEthanol was evaporated away
  10. 10
    workup.ADDITIONthe resulting residue was poured into 500 ml of 5% hydrochloric acid
  11. 11
    Otroa crystal was thus formed
  12. 12
    FiltraciónThe crystal taken out through filtration
  13. 13
    Otrowas recrystallized from a mixed solvent of ethanol and water

Procedimiento

17.4 g of ethyl 3-(4-hydroxyphenyl)propionate and 6.1 g of potassium hydroxide were added to 150 ml of ethanol, and stirred at 60° C. for 1 hour. This was cooled to 40° C., and 30 g of 3-[(tosyloxy)methyl]-3-ethyloxetane was dropwise added to it. Then, this was refluxed for 3 hours. Ethanol was evaporated away, and water and toluene were added to it for liquid-liquid separation. The toluene layer was washed with 3% hydrochloric acid, saturated sodium hydrogencarbonate and water, and then toluene was evaporated away. To the resulting residue, added were 20 g of sodium hydroxide, 100 ml of ethanol and 50 ml of water, and this was refluxed for 2 hours. Ethanol was evaporated away, and the resulting residue was poured into 500 ml of 5% hydrochloric acid, and a crystal was thus formed. The crystal taken out through filtration was recrystallized from a mixed solvent of ethanol and water, and 5 g of [4-(3-ethyloxetan-3-ylmethoxy)phenyl]propionic acid (OX7) was obtained. Its melting point was 85° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07407691B2uspto-grants-2008_08