Reacción #1552040

ord-ed1d01ef8e5e418a858c73634ac4968f

Ecuación de reacción

O=C(O)CCCCCCCCC(=O)O
sebacic acid
Oc1ccc(O)cc1
hydroquinone
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
C=COC(=O)CCCCCCCCC(=O)OC=C
sebacic acid divinyl ester

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe reaction mixture was refluxed for 4 hours
  2. 2
    Extracciónextracted with 150 ml 2N NaOH
  3. 3
    SecadoThe organic phase was dried over Na2SO4
  4. 4
    Otrothe volatile components were removed on a rotary evaporator
  5. 5
    OtroPurification by flash column chromatography on silica gel (PE:EE=10:1)
  6. 6
    Otroyielded 8.9 g (47% of th.) of a colorless liquid

Procedimiento

15 g (74.2 mmol) of sebacic acid, 0.66 g (2.06 mmol) of mercury(II)acetate, and 0.12 g of hydroquinone were precharged in 75 ml of vinyl acetate into a 250 ml three-necked flask and stirred for 20 minutes under argon. Then, 0.09 g (0.01 mol) of p-toluenesulfonic acid were added as a catalyst, and the reaction mixture was refluxed for 4 hours. After cooling down to room temperature, the obtained solution was diluted with 200 ml ethyl acetate and extracted with 150 ml 2N NaOH. The organic phase was dried over Na2SO4, and the volatile components were removed on a rotary evaporator. Purification by flash column chromatography on silica gel (PE:EE=10:1) yielded 8.9 g (47% of th.) of a colorless liquid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08999323B2uspto-grants-2015_04