Reaktion #2735

ord-e5b29654fa7b4c0a9addc6161d045c21

Reaktionsgleichung

CCOC(=O)c1ccc(O)cc1
ethyl 4-hydroxybenzoate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)=O
acetone
CCCCC#CC#CCOc1ccc(C(=O)OCC)cc1
ethyl 4-(2,4-nonadiynyloxy)-benzoate
Ausbeute 70.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturby heating for 11 hours
  2. 2
    Extraktionthe product was extracted with methylene chloride
  3. 3
    workup.DISTILLATIONAfter distilling off the solvent of the organic layer
  4. 4
    Sonstigethe residue formed
  5. 5
    Sonstigewas purified by a silica gel column chromatography(developing solvent

Vorschrift

In a flask were placed 3.78 g (0.024 mole) of 1-chloro-2,4-nonadiyne thus obtained, 3.32 g (0.02 mole) of ethyl 4-hydroxybenzoate, 5.5 g (0.04 mole) of potassium carbonate, and 50 ml of acetone and the mixture was refluxed by heating for 11 hours. After allowing to cool the reaction mixture to room temperature, the reaction mixture was poured in 250 ml of ice-water and the product was extracted with methylene chloride. After distilling off the solvent of the organic layer, the residue formed was purified by a silica gel column chromatography(developing solvent: hexane/ethyl acetate=3/1) to provide 4.0 g (yield 70%) of ethyl 4-(2,4-nonadiynyloxy)-benzoate.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05730903uspto-grants-1998_03