Реакция #955951

Уравнение реакции

4

5,5′-Bis((trimethylsilyl)ethynyl)-2,2′-bipyridine

KF

→

5,5′-diethynyl-2,2′-bipyridine

Растворители

MeOH

THF

Условия реакции

Обработка

1. 1
   ДругоеSubsequently, the solvents were removed under reduced pressure
2. 2
   workup.DISSOLUTIONThe residue was redissolved in 200 ml CH2Cl2
3. 3
   Промывкаwashed four times with 100 ml H2O each, in order
4. 4
   Другоеto remove inorganic salts
5. 5
   СушкаThe organic phase was dried over Na2SO4
6. 6
   Концентрированиеconcentrated under reduced pressure
7. 7
   Другоеpurified by silica flash column chromatography (eluent: CH2Cl2)
8. 8
   Другоеto yield a colorless powder of 204 mg (1.0 mmol, 81%) pure 5

Методика

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).

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