反应 #1747854
ord-feac67004ef7494a8768dbddaa96766a
反应方程式
反应条件
后处理
- 1其他(75° C.)
- 2过滤The precipitate was filtered off with suction
- 3洗涤washed successively with 125 ml of ethanol and hot water
- 4其他dried at 70° C. under reduced pressure
- 5温度The crude product (2.30 g) was heated
- 6温度under reflux in cyclohexane for two hours
- 7过滤After the hot suspension had been filtered
- 8其他the residue was dried
- 9workup.DISSOLUTIONdissolved in 40 ml of methylene chloride
- 10过滤filtered through a silica-
- 11workup.ADDITIONgel-filled glass fit
- 12其他After the solvent had been removed
- 13其他were obtained
实验过程
2.50 g (6.7 mmol) of 3,7-dibromo-10-methylphenothiazine (C. Bodea and M. Terdic, Acad. Rep. Rom. 1962, 13, 81-87), 1.85 g (14.9 mmol) of 98% phenylboronic acid, 0.11 g (0.14 mmol) of bis(triphenylphosphine)palladium dichloride and 1.03 g (7.4 mmol) of potassium carbonate were heated to boiling (75° C.) under reflux under nitrogen for 5 hours in 55 ml of dimethoxyethane and 28 ml of water. The reaction mixture was cooled to room temperature and stirred further overnight. The precipitate was filtered off with suction, washed successively with 125 ml of ethanol and hot water and dried at 70° C. under reduced pressure. The crude product (2.30 g) was heated to boiling under reflux in cyclohexane for two hours. After the hot suspension had been filtered, the residue was dried, dissolved in 40 ml of methylene chloride and filtered through a silica-gel-filled glass fit. After the solvent had been removed, 1.05 g (43% of theory) of light yellow, analytically pure solid having a melting point of 239-241° C. were obtained, whose solution in chloroform fluoresced at λ=464 nm.