Реакция #2006416

ord-479347c73df04b7e86de16f02bedb713

Уравнение реакции

C[O-].[Na+]
Sodium methoxide
O=Cc1ccc(C(=O)O)cc1
4-carboxybenzaldehyde
CC(=O)c1ccccc1
acetophenone
O=C(O)c1ccc(C=CC(=O)c2ccccc2)cc1
43
Выход 72.0%
O=C(O)c1ccc(C=CC(=O)c2ccccc2)cc1
4-(3-oxo-3-Phenylpropenyl)-benzoic Acid
Выход 72.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеhalf of the volume of methanol was removed under reduced pressure
  2. 2
    workup.ADDITIONThe mixture was poured into HCl 1M (50 mL) (until pH=2) and ethyl acetate
  3. 3
    workup.ADDITIONwas added
  4. 4
    ЭкстракцияThe separated aqueous layer was extracted with ethyl acetate (3×30 mL)
  5. 5
    Сушкаdried (MgSO4 anh.)
  6. 6
    Фильтрацияfiltered
  7. 7
    Другоеevaporated
  8. 8
    ДругоеThe residue was triturated with dichloromethane-hexanes (1:1)

Методика

Sodium methoxide (1.8 g, 33.3 mmol) was added to a stirred suspension of 4-carboxybenzaldehyde (2.5 g, 16.6 mmol) and acetophenone (2.0 g uL, 16.6 mmol) in methanol (50 mL) at room temperature. The mixture was stirred at room temperature for 16 hours, and half of the volume of methanol was removed under reduced pressure. The mixture was poured into HCl 1M (50 mL) (until pH=2) and ethyl acetate was added. The separated aqueous layer was extracted with ethyl acetate (3×30 mL) dried (MgSO4 anh.), filtered and evaporated. The residue was triturated with dichloromethane-hexanes (1:1) to afford 3 g of 43 (72% yield).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE043343E1uspto-grants-2012_05