Реакция #5092

ord-6737505c6dd04f6cbd916f255e400141

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGfurther stirred at room temperature for 1 hour
  2. 2
    Другоеthe crystals formed
  3. 3
    Фильтрацияwere collected by filtration
  4. 4
    ПромывкаThe crystals were washed with water and with n-hexane
  5. 5
    Другоеdried
  6. 6
    ДругоеRecrystallized from ethanol

Методика

10 Grams of 2,3-dihydro-4,6dimethyl-7-hydroxy-1H-inden-1-one was dissolved in 200 ml of dimethylformamide, then 5.45 g of 60%-sodium hydride was added gradually thereto and the reaction mixture was stirred at room temperature for 30 minutes. Next, 6.91 ml of p-anisaldehyde was added to the reaction mixture and further stirred at room temperature for 1 hour. The reaction mixture was poured into 500 ml of ice-water, then acidified by adding hydrochloric acid, and the crystals formed were collected by filtration. The crystals were washed with water and with n-hexane and dried. Recrystallized from ethanol to obtain 16.09 g of 2,3-dihydro-4,6-dimethyl-7-hydroxy-2-(4-methoxybenzylidene)-1H-inden-1-one. Yellow needle-like crystals. Melting point: 192°-193° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05242919uspto-grants-1993_09