反応 #1747855
ord-9e6756a91516456c96e1e3e0e10ba67a
反応方程式
反応物
試薬
反応条件
後処理
- 1ろ過filtered
- 2洗浄The residue was washed with 470 ml of ethanol and hot water
- 3その他dried at 70° C. under reduced pressure
- 4workup.DISSOLUTIONThe solid was dissolved in 100 ml of methylene chloride
- 5ろ過filtered through silica gel
- 6その他After the solvent had been removed under reduced pressure
- 7その他a tacky mass was obtained which
- 8その他crystallized
- 9workup.STIRRINGwith stirring overnight
- 10ろ過The crystals were filtered off with suction
- 11洗浄washed with 300 ml of methanol
- 12その他dried at 40° C. under reduced pressure
- 13その他were obtained
- 14その他The crude product was recrystallized twice from ethyl acetate
- 15その他were obtained
実験手順
9.30 g (25.1 mmol) of 3,7-dibromo-10-methylphenothiazine, 9.50 g (55.2 mmol) of 1-naphthylboronic acid, 0.407 g (0.50 mmol) of bis(triphenylphosphane)palladium dichloride and 3.80 g (27.5 mmol) of potassium carbonate were heated to boiling under reflux under nitrogen for 5 hours in 204 ml of dimethoxyethane and 101 ml of water. The reaction mixture was cooled to room temperature, stirred further overnight and then filtered. The residue was washed with 470 ml of ethanol and hot water, and dried at 70° C. under reduced pressure. The solid was dissolved in 100 ml of methylene chloride and filtered through silica gel. After the solvent had been removed under reduced pressure, a tacky mass was obtained which, after 200 ml of methanol had been added, crystallized with stirring overnight. The crystals were filtered off with suction, washed with 300 ml of methanol and dried at 40° C. under reduced pressure. 10.33 g of light yellow microcrystals having a melting point of 185-190° C. were obtained. The crude product was recrystallized twice from ethyl acetate. 5.71 g (49% of theory) of analytically pure, almost colorless microcrystals having a melting point of 191-194° C. were obtained, whose solution in chloroform fluoresced at λ=468 nm.