Reacción #452432

ord-6dfb67eadeae4045b0c4481d0500b39c

Ecuación de reacción

O=C1CCC2(CC1)OCCO2
1,4-cyclohexanedione mono-ethylene ketal
CNC
dimethylamine
[BH3-]C#N.[Na+]
sodium cyanoborohydride
CN(C)C1CCC2(CC1)OCCO2
title compound
Rendimiento 85.0%
CN(C)C1CCC2(CC1)OCCO2
4-dimethylamino-1-cyclohexanone ethylene ketal
Rendimiento 85.0%

Condiciones de reacción

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

Tratamiento posterior

  1. 1
    workup.STIRRINGthe reaction stirred for an additional hour at ambient
  2. 2
    workup.STIRRINGstirred 18 hours at ambient
  3. 3
    OtroThe volatiles were removed under reduced pressure
  4. 4
    workup.DISSOLUTIONthe residue dissolved in cold 5% tartaric acid solution
  5. 5
    ExtracciónThis aqueous phase was extracted well with dichloromethane
  6. 6
    Concentraciónconcentrated under reduced pressure

Procedimiento

To a solution of 5.0 gm (32 mMol) 1,4-cyclohexanedione mono-ethylene ketal and 10.80 gm (240 mMol) dimethylamine were added 2.0 mL acetic acid and the mixture was stirred at 0° C. for 1.5 hours. To this solution were then added 3.62 gm (58 mMol) sodium cyanoborohydride and the reaction stirred for an additional hour at ambient. The pH of the reaction mixture was adjusted to ~7 with 16 mL acetic acid and stirred 18 hours at ambient. The volatiles were removed under reduced pressure and the residue dissolved in cold 5% tartaric acid solution and then the aqueous phase was made basic with 5N sodium hydroxide. This aqueous phase was extracted well with dichloromethane. These organic extracts were combined and concentrated under reduced pressure to give 5.04 gm (85%) of the title compound as an oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06126932uspto-grants-2000_10