Reacción #1994246

ord-534a07c08e2640db9a0d12b4b74efbf0

Ecuación de reacción

C=CCC(CC=C)C(=O)OCC
2-allylpent-4-enoic acid ethyl ester
[Na+].[OH-]
sodium hydroxide
C=CCC(CC=C)C(=O)O
2-allylpent-4-enoic acid
Rendimiento 54.2%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheated
  2. 2
    Temperaturaat reflux temperature for 2 hours
  3. 3
    Otrosolvent was removed at reduced pressure
  4. 4
    workup.ADDITIONTo the residue were added 75 mL of diethyl ether and 10 mL of concentrated hydrochloric acid
  5. 5
    workup.STIRRINGThe mixture was stirred at room temperature for 10 minutes
  6. 6
    Otrothe layers were separated
  7. 7
    Secadothe diethyl ether layer was dried over magnesium sulfate
  8. 8
    FiltraciónAfter filtration
  9. 9
    Otroto remove the magnesium sulfate, solvent
  10. 10
    Otrowas removed at reduced pressure

Procedimiento

To a stirred solution of 2-allylpent-4-enoic acid ethyl ester (prepared above, 9.0 g, 54 mmol) in 50 mL of methanol and 2 mL of water was added sodium hydroxide (2.5 g, 63 mmol, available from EMD). The solution was stirred for 15 hours, then heated at reflux temperature for 2 hours. After cooling the reaction mixture to room temperature, solvent was removed at reduced pressure. To the residue were added 75 mL of diethyl ether and 10 mL of concentrated hydrochloric acid. The mixture was stirred at room temperature for 10 minutes, then the layers were separated and the diethyl ether layer was dried over magnesium sulfate. After filtration to remove the magnesium sulfate, solvent was removed at reduced pressure to leave 4.1 g of 2-allylpent-4-enoic acid as a colorless oil whose structure was confirmed by NMR analyses.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08597784B2uspto-grants-2013_12