Réaction #848

ord-c218088b16c541088a933a7606f68c4c

Équation de réaction

O=C(O)c1ccc(O)cc1
p-hydroxybenzoic acid
CCCCCCCCCC(=O)Cl
decanoic acid chloride
c1ccncc1
pyridine
CCCCCCCCCC(=O)Oc1ccc(C(=O)O)cc1
p-decanoyloxybenzoic acid

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionan organic layer was extracted with dichloromethane
  2. 2
    LavageThe organic layer was washed with 1N hydrochloric acid
  3. 3
    Séchagedried over anhydrous sodium sulfate
  4. 4
    workup.DISTILLATIONthe solvent was distilled off
  5. 5
    Lavageresidue was washed with n-hexane
  6. 6
    Autredried
  7. 7
    Autreto give a crude end product

Mode opératoire

10 Grams of p-hydroxybenzoic acid and 15 g of decanoic acid chloride were stirred at room temperature, and 7.2 g of pyridine was dropwise added. After the mixture was stirred for 1 day, a reaction product was poured into water, and an organic layer was extracted with dichloromethane. The organic layer was washed with 1N hydrochloric acid and dried over anhydrous sodium sulfate, the solvent was distilled off, and then residue was washed with n-hexane and then dried to give a crude end product.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05723069uspto-grants-1998_03