Реакция #1135825

ord-11a6a4630b6044f995f11a0c8ff7225a

Уравнение реакции

COc1ccc(C2=C(c3ccc(O)cc3)COc3cc(O)ccc32)cc1
product
COc1ccc(C2=C(c3ccc(O)cc3)COc3cc(O)ccc32)cc1
3-(4-hydroxyphenyl)-4-(4-methoxyphenyl)-2H-chromen-7-ol
CCO
ethanol
COc1ccc(C2c3ccc(O)c(C)c3OCC2c2ccc(O)cc2)cc1
3-(4-hydroxyphenyl)-4-(4-methoxyphenyl)-8-methyl-3,4-dihydro-2H-chromen-7-ol

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеfor 3 hours
  2. 2
    ФильтрацияThe reaction was filtered through Celite
  3. 3
    Другоеto remove the catalyst
  4. 4
    Промывкаrinsed through with ethanol (100 ml)
  5. 5
    КонцентрированиеThe filtrate was concentrated to ˜15 ml
  6. 6
    workup.ADDITIONbefore being poured
  7. 7
    Температураinto chilled
  8. 8
    ДругоеA pale orange precipitate formed which
  9. 9
    Другоеthen formed a brown oil
  10. 10
    ЭкстракцияThe mixture was then extracted with diethyl ether
  11. 11
    Промывкаthe combined organic layers washed with water (3×100 ml), brine (1×100 ml)
  12. 12
    Сушкаdried over anhydrous magnesium sulphate
  13. 13
    Фильтрацияfiltered
  14. 14
    ДругоеThe solvent was removed in vacuo
  15. 15
    Другоеto give red/brown oil
  16. 16
    ДругоеThe product was recrystallised from diethyl ether (˜15 ml)
  17. 17
    Другоеto give brown solid which
  18. 18
    Промывкаwas rinsed with chilled diethyl ether
  19. 19
    Другоеto give off-white crystals

Методика

2.5 g of the product of step 8, 10% Pd/Al2O3 0.4 g and 50 ml of ethanol were combined in a 2-neck 100 ml round bottom flask. The reaction was hydrogenated at low pressure using standard conditions for 3 hours. The reaction was filtered through Celite to remove the catalyst, rinsed through with ethanol (100 ml). The filtrate was concentrated to ˜15 ml before being poured into chilled, stirred water (300 mL). A pale orange precipitate formed which then formed a brown oil. The mixture was then extracted with diethyl ether, the combined organic layers washed with water (3×100 ml), brine (1×100 ml), dried over anhydrous magnesium sulphate and filtered. The solvent was removed in vacuo to give red/brown oil. The product was recrystallised from diethyl ether (˜15 ml), to give brown solid which was rinsed with chilled diethyl ether to give off-white crystals. 4 crops of (IV), ˜1 g. The 1H NMR spectrum and numbering scheme being shown below.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09381186B2uspto-grants-2016_07