Реакция #155321

ord-228a7720349040428aec09930e7b044a

Уравнение реакции

COCCOC
dimethoxyethane
CCCOc1cc2ccccc2c2c(=O)cc(I)[nH]c12
3-Iodo-5-propoxy-4H-benzo[f]quinolin-1-one
O
water
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CCCOc1cc2ccccc2c2c(=O)c(-c3ccoc3)c[nH]c12
2-furan-3-yl-5-propoxy-4H-benzo[f]quinolin-1-one
Выход 48.0%

Условия реакции

Температура
95°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction mixture was cooled to room temperature
  2. 2
    Экстракцияthe resulting mixture was subjected to extraction
  3. 3
    КонцентрированиеThe thus-obtained organic layer was concentrated under reduced pressure
  4. 4
    Другоеthe residue was purified
  5. 5
    КонцентрированиеThe purified product was concentrated under reduced pressure
  6. 6
    Промывкаthe residue was washed with ethyl acetate
  7. 7
    Другоеdried

Методика

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%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE045108E1uspto-grants-2014_09