Reacción #452446

ord-c5099169b4f64c9aa796582ef8226ea4

Ecuación de reacción

[Cl-].[NH4+]
Ammonium chloride
[NH4+].[OH-]
ammonium hydroxide
C=CC(C)(CCC=C(C)C)OC(=O)CC(C)=O
3,7-Dimethyl-1,6-octadien-3-yl 3-oxo-butyrate
Cl
HCl
[Ca+2].[OH-].[OH-]
Calcium hydroxide
CCCCCCC(=O)Cl
Heptanoyl chloride
C=CC(C)(CCC=C(C)C)OC(=O)CC(=O)CCCCCC
desired compound
C=CC(C)(CCC=C(C)C)OC(=O)CC(=O)CCCCCC
3,7-dimethyl-1,6-octadien-3-yl 3-(hexyl)-3-oxo-propionate

Condiciones de reacción

Temperatura
37.5°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrofitted with an internal thermometer, addition funnel, condenser and argon inlet
  2. 2
    Otrobetween 35-40° C
  3. 3
    workup.ADDITIONis added to the flask
  4. 4
    workup.WAITAfter 20 min
  5. 5
    workup.WAITAfter 1 h
  6. 6
    workup.WAITAfter 1 h
  7. 7
    OtroThe layers are separated
  8. 8
    Extracciónthe aqueous phase extracted with 100 mL of dichloromethane
  9. 9
    LavadoThe combine organic layers are washed with saturated NaHCO3 solution, water
  10. 10
    Secadodried over MgSO4
  11. 11
    Filtraciónfiltered
  12. 12
    Concentraciónconcentrated by rotary evaporation
  13. 13
    Otropurified by flash chromatography

Procedimiento

3,7-Dimethyl-1,6-octadien-3-yl 3-oxo-butyrate (30.00 g, 0.126 mol), dichloromethane (50 mL) and methyl ethyl ketone (10 mL) are combined in a 500 mL three-necked round-bottomed flask fitted with an internal thermometer, addition funnel, condenser and argon inlet. Calcium hydroxide (9.80 g, 0.132 mol, powdered) is added to the flask and the slurry stirs for 1 h. Heptanoyl chloride (17.84 g, 0.120 mol) in 10 ml of dichloromethane is added over 15 min so as to keep the reaction temperature between 35-40° C. The reaction continues to stir at 35-40° C. for 2 h. Ammonium chloride (7.06 g, 0.132 mol) dissolved in 20 mL of water is added to the flask. After 20 min, concentrated ammonium hydroxide is added to the mixture to adjust the pH to ~9.0. After 1 h, 20% HCl solution is added to drop the pH to ~1.0. After 1 h, the mixture is poured into 300 mL of dichloromethane. The layers are separated and the aqueous phase extracted with 100 mL of dichloromethane. The combine organic layers are washed with saturated NaHCO3 solution, water, dried over MgSO4, filtered, concentrated by rotary evaporation and purified by flash chromatography to yield the desired compound. Structure is confirmed my 1H and 13C NMR.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06126953uspto-grants-2000_10