Reacción #2146733

ord-bbafd291e0814f8194d482de053075ac

Ecuación de reacción

CC(C)(C)[O-].[K+]
potassium tert-butoxide
C1CCOC1
THF
C1CCOC1
THF
CC(=O)OCCC(C)CC=O
3-methyl-5-oxopentyl acetate
C1CCOC1
THF
CCC/C=C\CC(C)CCOC(C)=O
(5Z)-3-methylnon-5-enyl acetate
Rendimiento 78.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONAfter complete addition
  2. 2
    workup.STIRRINGStirring
  3. 3
    workup.WAITwas continued a further 15 min at −10° C., before the cooling bath
  4. 4
    Otrowas removed
  5. 5
    workup.STIRRINGAfter 3 h of stirring at room temp.
  6. 6
    workup.ADDITIONthe reaction mixture was poured into 1 L of water
  7. 7
    Otrothe organic layer separated
  8. 8
    Extracciónaqueous one extracted twice with 1 L of ether each
  9. 9
    LavadoThe combined organic extracts were washed with water and brine
  10. 10
    Secadodried with sodium sulphate
  11. 11
    Concentraciónconcentrated under reduced pressure
  12. 12
    OtroThe crude material (191 g) was purified by flash chromatography (1.00 kg of silica gel, pentane/ether, 19:1, Rf=0.40)

Procedimiento

Under an atmosphere of nitrogen, a solution of 46.3 g (413 mmol) of potassium tert-butoxide in 250 mL of dry THF was a added between −15° C. and −10° C. to a stirred mixture of 150 g (376 mmol) butyl triphenylphosphonium bromide in 500 mL of dry THF. After complete addition, stirring was continued at −10° C. for 30 min, prior to the dropwise addition of 65.3 g (413 mmol) of 3-methyl-5-oxopentyl acetate in 250 mL of dry THF within a period of 30 min. Stirring was continued a further 15 min at −10° C., before the cooling bath was removed and the reaction mixture was allowed to warm to room temp. After 3 h of stirring at room temp., the reaction mixture was poured into 1 L of water, the organic layer separated and aqueous one extracted twice with 1 L of ether each. The combined organic extracts were washed with water and brine, dried with sodium sulphate, and concentrated under reduced pressure. The crude material (191 g) was purified by flash chromatography (1.00 kg of silica gel, pentane/ether, 19:1, Rf=0.40) to afford 57.9 g (78%) of (5Z)-3-methylnon-5-enyl acetate as a colourless liquid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08278230B2uspto-grants-2012_10