Réaction #1552040

ord-ed1d01ef8e5e418a858c73634ac4968f

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08999323B2uspto-grants-2015_04