Reaktion #1675320

ord-4fbef54a6bf0459291a9c374ec5c8b2c

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeAfter the completion of the reaction
  2. 2
    Sonstigethe solvent was removed by evaporation under reduced pressure
  3. 3
    Sonstigethe residue obtained
  4. 4
    Sonstigewas purified by means of a preparative thin layer chromatography [adsrobent: "Silica gel 60 F254 " manufactured by E. Merck A. G., developing solvent: benzene-ethyl acetate (5:1 mixture by volume/volume)]

Vorschrift

9 Milligrams of 1,16-bis(2,5-dimethoxy-1,4-benzoquinon-3-yl)-cis-8-hexadecene was dissolved in 1 ml of methylene chloride, then to this solution was added 8 mg of m-chlorobenzoic acid and the mixture was stirred at room temperature for 1 hour. After the completion of the reaction, the solvent was removed by evaporation under reduced pressure, and the residue obtained was purified by means of a preparative thin layer chromatography [adsrobent: "Silica gel 60 F254 " manufactured by E. Merck A. G., developing solvent: benzene-ethyl acetate (5:1 mixture by volume/volume)] to obtain 3 mg of 1,16-bis(2,5-dimethoxy-1,4-benzoquinon-3-yl)-8,9-epoxyhexadecane. Yellow oily substance.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05220042uspto-grants-1993_06