Reacción #487504

ord-9569a0fca728472ab89020adcb2b87f5

Ecuación de reacción

CC(C)O
isopropyl alcohol
CC(C)O
isopropyl alcohol
CC(=O)OCC#CCCCCO[Si](C)(C)C(C)(C)C
( 28 )
CC(=O)OCC#CCCCCO[Si](C)(C)C(C)(C)C
Acetic acid 7-(tert-butyl-dimethyl-silanyloxy)-hept-2-ynyl ester
CC(C)=O.O=S(=O)(O)O.[O]=[Cr](=[O])=[O]
Jones Reagent
CC(=O)OCC#CCCCC(=O)O
oil
CC(=O)OCC#CCCCC(=O)O
7-Acetoxy-hept-5-ynoic acid

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled with an ice bath
  2. 2
    workup.ADDITIONwas added
  3. 3
    workup.WAITAfter another 15 minutes
  4. 4
    Filtraciónwas filtered through celite
  5. 5
    Otrothe filtrate evaporated in vacuo
  6. 6
    OtroThe residue was partitioned between 100 mL ether and 100 mL saturated ammonium chloride solution
  7. 7
    ExtracciónThe aqueous layer was extracted with 100 mL ether
  8. 8
    Lavadothe combined ether solution washed with brine
  9. 9
    Secadodried (MgSO4)
  10. 10
    Filtraciónfiltered
  11. 11
    Otroevaporated

Procedimiento

A solution of crude (28) in acetone (100 mL) was treated with Jones Reagent (18.0 mL, 41.4 mmol, 2.3 M) and cooled with an ice bath. After 1 hour at room temperature, 10 mL isopropyl alcohol was added and the mixture stirred for 15 minutes. The mixture still had a brown color so another 10 mL isopropyl alcohol was added. After another 15 minutes, the color had not changed so the mixture was filtered through celite and the filtrate evaporated in vacuo. The residue was partitioned between 100 mL ether and 100 mL saturated ammonium chloride solution. The aqueous layer was extracted with 100 mL ether and the combined ether solution washed with brine and then dried (MgSO4), filtered and evaporated to leave a yellow oil (6.333 g) that was used directly in the next step.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08741281B2uspto-grants-2014_06