Réaction #833522

ord-a3c615700c3d452b95de9d06cf0e6bc0

Équation de réaction

O=S(=O)(O)O
Sulfuric acid
O=C(O)CCc1ccc(O)cc1
3-(4-hydroxyphenyl)propionic acid
CCO
ethanol
CCOC(=O)CCc1ccc(O)cc1
ethyl 3-(4-hydroxyphenyl)propionate

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurerefluxed successively for 5 hours
  2. 2
    ConcentrationThe reaction mixture was concentrated
  3. 3
    workup.ADDITIONthe obtained concentrated solution was poured into water (1,000 mL)
  4. 4
    AutreAfter separation of the solution
  5. 5
    Lavagewashed with a small amount of water
  6. 6
    Séchagedried over anhydrous magnesium sulfate
  7. 7
    workup.DISTILLATIONEthyl acetate and unreacted ingredients were distilled off from the ethyl acetate layer
  8. 8
    Autreto obtain concentrates (1,400 g)
  9. 9
    workup.DISTILLATIONThe concentrates were purified by distillation under a reduced pressure

Mode opératoire

Sulfuric acid (230 g) was dropped under stirring for 10 minutes to an ethanol solution (1500 mL) of 3-(4-hydroxyphenyl)propionic acid (1150 g), and refluxed successively for 5 hours. The reaction mixture was concentrated and the obtained concentrated solution was poured into water (1,000 mL) and stirred with addition of ethyl acetate. After separation of the solution, an ethyl acetate layer was neutralized with an aqueous solution of a saturated sodium carbonate, washed with a small amount of water and then dried over anhydrous magnesium sulfate. Ethyl acetate and unreacted ingredients were distilled off from the ethyl acetate layer to obtain concentrates (1,400 g). The concentrates were purified by distillation under a reduced pressure to obtain ethyl 3-(4-hydroxyphenyl)propionate (1,144 g). The boiling point was 160° C./4.0 hPa.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07393569B2uspto-grants-2008_07