Реакция #2348122
ord-94d45aab2d0c4d6e88a436fb64fbf189
Уравнение реакции
Реактанты
Реагенты
Условия реакции
Обработка
- 1ДругоеThe cooled reaction mixture
- 2Экстракцияthe neutral components were extracted with ether (3×50 mL)
- 3Экстракцияextracted with ether (2×50 mL)
- 4ДругоеThe solid was isolated by filtration
- 5Промывкаwashed with water (100 mL), ethyl acetate (50 mL) and ether (30 mL)
- 6Другоеair-dried
Методика
The trans-stilbene (1.17 g, 4.85 mmol) was dissolved in dry NMP (12 mL). Thiophenol (1.07 g, 9.7 mmol) was then added to the above solution, followed by addition of K2CO3 (67 mg, 0.48 mmol). The resulting mixture was heated for 8 hours at 195° C. under nitrogen. The cooled reaction mixture was made alkaline with 1 N NaOH (pH=10), and the neutral components were extracted with ether (3×50 mL). The aqueous layer was acidified to pH=4 with 1 N HCl and stirred at room temperature for 30 minutes, and extracted with ether (2×50 mL). Then pH was adjusted to pH=8 with saturated NaHCO3. The solid was isolated by filtration, washed with water (100 mL), ethyl acetate (50 mL) and ether (30 mL), and air-dried to yield 5-[(E)-2-(4-hydroxyphenyl)-vinyl]-pyridin-2-ol (715 mg, 69%). MS (ES) m/z: 214.08 (M+1); 13C-NMR (DMSO-d6): δ 162.42, 157.50, 138.21, 134.07, 129.04, 127.92, 125.67, 121.59, 121.03, 116.89, and 116.18.