Reacción #1000

ord-02e021bf3546479584ca183e01838f59

Ecuación de reacción

C1CCOC1
tetrahydrofuran
[BH4-].[Na+]
sodium borohydride
[Cl-].[Na+]
sodium chloride
C1=CC2(CCCC1)OCCO2
2-cycloheptenone ethylene ketal
OC1CCCCC2(C1)OCCO2
3-hydroxycycloheptanone ethylene ketal

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto give a suspension
  2. 2
    Temperaturathe mixture was cooled in an ice water bath
  3. 3
    Otroto reach ambient temperature
  4. 4
    workup.STIRRINGstirred overnight
  5. 5
    workup.STIRRINGstirred for 30 minutes
  6. 6
    Otrothe solution was decanted into brine
  7. 7
    Extracciónextracted with ethyl acetate
  8. 8
    Secadodried over sodium sulfate
  9. 9
    Filtraciónfiltered
  10. 10
    Concentraciónconcentrated in vacuo

Procedimiento

Mercury(II) acetate (80.7 g, 0.25 mol) was dissolved in water (150 mL), then tetrahydrofuran (150 mL) was added to give a suspension. To this stirring suspension was added 2-cycloheptenone ethylene ketal (39 g, 0.25 mol). After stirring at ambient temperature for 3 hours, the mixture was cooled in an ice water bath. A 10% aqueous sodium hydroxide solution (150 mL) was added, followed by a solution of sodium borohydride (4.8 g, 0.13 mol) in 10% aqueous sodium hydroxide (150 mL). The mixture was allowed to reach ambient temperature and stirred overnight. The mixture was saturated with sodium chloride, stirred for 30 minutes, then allowed to settle; the solution was decanted into brine and extracted with ethyl acetate, dried over sodium sulfate, filtered, and concentrated in vacuo to give 3-hydroxycycloheptanone ethylene ketal (36 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723462uspto-grants-1998_03