Reaktion #5645
ord-a5d5033460474ef09b7089853a326df4
Reaktionsgleichung
2,4-dimethoxybenzaldehyde
potassium hydroxide
HCl
2-acetylfuran
→
1,5-Di(2-furyl)-3-(2,4-dimethoxyphenyl)-1,5-pentanedione
Reagenzien
Keine
Reaktionsbedingungen
Temperatur
55°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1TemperaturThe resulting mixture was heated
- 2Temperaturto reflux
- 3Extraktionextracted with CH2Cl2
- 4TrocknenThe CH2Cl2 extracts were dried (Na2SO4)
- 5Sonstigethe solvents removed at high vacuum
- 6workup.WAITon standing overnight
- 7Sonstigeaffording 36.7 g of crude dione 3
Vorschrift
Following the general methods outlined by Weller and Luellen (see above), to a solution of 16.6 g (0.1 mole) of 2,4-dimethoxybenzaldehyde 1 and 20 ml (0.2 mole) of 2-acetylfuran 2 in 100 ml of methanol was added 5.5 g of potassium hydroxide previously dissolved in a small amount of methanol. The resulting mixture was heated to reflux and then stirred overnight at 55° C. The solution was then poured into water acidified with 1N HCl and extracted with CH2Cl2. The CH2Cl2 extracts were dried (Na2SO4) and the solvents removed at high vacuum. The resulting amber oil solidified on standing overnight affording 36.7 g of crude dione 3.