تفاعل #955951
ord-1513561857dc4ebeb902cb5959c561aa
معادلة التفاعل
الكواشف
ظروف التفاعل
المعالجة
- 1أخرىSubsequently, the solvents were removed under reduced pressure
- 2workup.DISSOLUTIONThe residue was redissolved in 200 ml CH2Cl2
- 3غسيلwashed four times with 100 ml H2O each, in order
- 4أخرىto remove inorganic salts
- 5تجفيفThe organic phase was dried over Na2SO4
- 6تركيزconcentrated under reduced pressure
- 7أخرىpurified by silica flash column chromatography (eluent: CH2Cl2)
- 8أخرىto yield a colorless powder of 204 mg (1.0 mmol, 81%) pure 5
الإجراء التجريبي
4 (390 mg, 1.12 mmol) was dissolved in a mixture of 40 ml MeOH and 10 ml THF; then KF powder (400 mg, 6.88 mmol) was added and the solution was stirred at room temperature overnight. Subsequently, the solvents were removed under reduced pressure. The residue was redissolved in 200 ml CH2Cl2 and washed four times with 100 ml H2O each, in order to remove inorganic salts. The organic phase was dried over Na2SO4, concentrated under reduced pressure and purified by silica flash column chromatography (eluent: CH2Cl2) to yield a colorless powder of 204 mg (1.0 mmol, 81%) pure 5. 1H NMR (CDCl3, 250 MHz): δ=8.76 (d, 2H, JHH=1.0 Hz, bpy-H), 8.39 (d, 2H, JHH=6.0 Hz, bpy-H), 7.90 (dd, 2H, JHH=1.1 Hz, 5.1 Hz, bpy-H), 3.31 (s, 2H, bpy-CCH).