Reaktion #74966

ord-ea2aaea7fcb84ecf97673d17fa69c1c4

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeprepared
  2. 2
    SonstigeThe resulting reaction mixture
  3. 3
    workup.STIRRINGwas continuously stirred
  4. 4
    Temperaturrefluxed vigorously for 8.5 hours
  5. 5
    TemperaturAfter cooling the mixture to 0° C.
  6. 6
    Filtrationit was filtered
  7. 7
    Waschenthe crude solid was washed with cold Skellysolve
  8. 8
    SonstigeThe product was recrystallized from a mixture of 1000 ml

Vorschrift

A mixture of 256 grams (0.62 mol.) of 1,2,3,4,6,9,9-heptachloro-1,4,4a,8a-tetrahydro-1,4-methanonaphthalene-5,8-dione, prepared according to Example 24, and 500 ml. of methanol in a 2 liter reaction flask was stirred at room temperature while air in the reaction vessel was swept out with nitrogen. Six ml. of pyridine was then added to the liquid-solid mixture. The resulting reaction mixture was continuously stirred, and refluxed vigorously for 8.5 hours. After cooling the mixture to 0° C., it was filtered, and the crude solid was washed with cold Skellysolve. Yield 121 grams. The product was recrystallized from a mixture of 1000 ml. of Skellysolve and 250 ml. of acetone. M.P. 120.5°-122° C. The product has the following structure: ##STR57##

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04174457uspto-grants-1979_11