Reacción #2006416

Ecuación de reacción

Sodium methoxide

4-carboxybenzaldehyde

acetophenone

→

43

Rendimiento 72.0%

4-(3-oxo-3-Phenylpropenyl)-benzoic Acid

Rendimiento 72.0%

Disolventes

methanol

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrohalf 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
   ExtracciónThe separated aqueous layer was extracted with ethyl acetate (3×30 mL)
5. 5
   Secadodried (MgSO4 anh.)
6. 6
   Filtraciónfiltered
7. 7
   Otroevaporated
8. 8
   OtroThe residue was triturated with dichloromethane-hexanes (1:1)

Procedimiento

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).

Fuente