反応 #155321
ord-228a7720349040428aec09930e7b044a
反応方程式
反応物
試薬
反応条件
後処理
- 1温度The reaction mixture was cooled to room temperature
- 2抽出the resulting mixture was subjected to extraction
- 3濃縮The thus-obtained organic layer was concentrated under reduced pressure
- 4その他the residue was purified
- 5濃縮The purified product was concentrated under reduced pressure
- 6洗浄the residue was washed with ethyl acetate
- 7その他dried
実験手順
3-Iodo-5-propoxy-4H-benzo[f]quinolin-1-one (1.06 g, 2.79 mmol) was suspended in dimethoxyethane (20 ml). Furan-3-boron acid (354 mg, 3.16 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II)-dichloromethane complex (PdCl2(DPPF).CH2Cl2, 123 mg, 0.11 mmol) and a 2N aqueous sodium carbonate solution (4.0 ml) were sequentially added to the suspension. The mixture was stirred at 90 to 100° C. under a nitrogen atmosphere for hours. The reaction mixture was cooled to room temperature, water was added thereto, and the resulting mixture was subjected to extraction using dichloromethane. The thus-obtained organic layer was concentrated under reduced pressure, and the residue was purified using silica gel column chromatography (dichloromethane:ethyl acetate=80:1). The purified product was concentrated under reduced pressure, the residue was washed with ethyl acetate and then dried, giving a pale brown powder of 2-furan-3-yl-5-propoxy-4H-benzo[f]quinolin-1-one (430 mg, yield: 48%).