Réaction #452432

ord-6dfb67eadeae4045b0c4481d0500b39c

Équation de réaction

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
Rendement 85.0%
CN(C)C1CCC2(CC1)OCCO2
4-dimethylamino-1-cyclohexanone ethylene ketal
Rendement 85.0%

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06126932uspto-grants-2000_10