Реакция #54508

ord-e13f36d1f3a648878cd8800005964c27

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.DISSOLUTIONto dissolve the organic matter and air
  2. 2
    Другоеwas then bubbled through the solution for 3 hours
  3. 3
    ЭкстракцияThe resulting solution was extracted with 100 parts petroleum ether (twice),
  4. 4
    Экстракцияre-extracted with diethylether
  5. 5
    ЭкстракцияThe ether extract
  6. 6
    Промывкаwas washed with saturated sodium chloride
  7. 7
    Сушкаdried over magnesium sulfate
  8. 8
    Другоеevaporated
  9. 9
    Фильтрацияfiltered
  10. 10
    ДругоеThe filtrate was evaporated to dryness
  11. 11
    Другоеthe residue triturated with petroleum ether

Методика

Four parts of crude ethyl 2-[(2-methylphenyl)acetyl]tetradecanoate obtained in Example 3 was combined with 12 parts of cold concentrated sulfuric acid and stirred at room temperature for 66 hours. The mixture was poured into ice water and made slightly basic by the addition of 50% aqueous sodium hydroxide. Enough ethanol was added to dissolve the organic matter and air was then bubbled through the solution for 3 hours. The resulting solution was extracted with 100 parts petroleum ether (twice), acidified with hydrochloric acid and re-extracted with diethylether. The ether extract was washed with saturated sodium chloride, dried over magnesium sulfate and evaporated. The residue was taken up in acetonitrile and filtered. The filtrate was evaporated to dryness and the residue triturated with petroleum ether to give 0.2 g of 2-dodecyl-3-hydroxy-5-methyl-1,4-napthoquinone, m.p. 92°-93° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04148918uspto-grants-1979_04