Reacción #9896

ord-aade5df588aa4d7984bc144871052427

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónconcentrated
  2. 2
    workup.ADDITIONWater was added to the residue
  3. 3
    ExtracciónThe aqueous layer was extracted with ether
  4. 4
    LavadoThe combined organic layers were washed with water
  5. 5
    Otrodried
  6. 6
    Concentraciónconcentrated

Procedimiento

A solution of ε-caprolactone (11.4 g, 0.100 mol), MeOH (300 mL) and concentrated H2SO4 (5 mL) was refluxed overnight. The resulting mixture was cooled to room temperature and concentrated. Water was added to the residue and the pH was adjusted to 7 with solid NaHCO3. The aqueous layer was extracted with ether. The combined organic layers were washed with water, dried and concentrated to give 6-hydroxy-hexanoic acid methyl ester as a colorless oil, which was used in the next step without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091357B2uspto-grants-2006_08