Reacción #2473

ord-cb6326117e3045cb93e4c9a0471e9b58

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe ether phase was separated
  2. 2
    Extracciónthe aqueous phase once more extracted with ether
  3. 3
    LavadoThe combined organic phases were washed with water
  4. 4
    Secadodried over MgSO4
  5. 5
    Filtraciónfiltered
  6. 6
    Concentraciónconcentrated
  7. 7
    workup.DISTILLATIONThe residue was distilled in a bulb-to-bulb apparatus (oven t.: 180°/7 Pa)

Procedimiento

To 104 mg (0.49 mmole) of (±)cis-3-oxo-2-pentyl-1-cyclopentaneacetic acid (93:7 cis/trans ratio) in 1 ml of (CH3)2CO there were added, first 56 μl of (CH3)2SO4 (74 ml, 0.59 mmole, 1.2 eq.) and then 81 mg (0.59 mmole, 1.2 eq.) of anhydrous solid K2 CO3. The resulting suspension was heated at r.t. during 4 h and taken in water and with ether. The ether phase was separated and the aqueous phase once more extracted with ether. The combined organic phases were washed with water, dried over MgSO4, filtered and concentrated. The residue was distilled in a bulb-to-bulb apparatus (oven t.: 180°/7 Pa) to provide 93 mg (0.44 mmole, yield 84%) of methyl (±)-cis-3-oxo-2-pentyl-1-cyclopentaneacetate (92/8 cis/trans ratio).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05728866uspto-grants-1998_03